The following is a conversation with Dimitri Korkin,
his second time in the podcast.
He's a professor of bioinformatics
and computational biology at WPI,
where he specializes in bioinformatics
of complex disease, computational genomics,
systems biology, and biomedical data analytics.
He loves biology, he loves computing,
plus he is Russian and recites a poem in Russian
at the end of the podcast.
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And now here's my conversation with Dimitri Korkin.
It's often said that proteins and the amino acid residues
that make them up are the building blocks of life.
Do you think of proteins in this way
as the basic building blocks of life?
Yes and no.
So the proteins indeed is the basic unit,
biological unit that carries out
important function of the cell.
However, through studying the proteins
and comparing the proteins across different species,
across different kingdoms,
you realize that proteins are actually
much more complicated.
So they have so-called modular complexity.
And so what I mean by that is an average protein
consists of several structural units.
So we call them protein domains.
And so you can imagine a protein as a string of beads
where each bead is a protein domain.
And in the past 20 years,
scientists have been studying the nature
of the protein domains.
Cause we realize that it's the unit.
Because if you look at the functions, right?
So many proteins have more than one function.
And those protein functions are often carried out
by those protein domains.
So we also see that in the evolution,
those proteins domains get shuffled.
So they act actually as a unit.
Also from the structural perspective, right?
So, you know, some people think of a protein
as a sort of a globular molecule.
But as a matter of fact is the globular part
of this protein is a protein domain.
So we often have this, you know,
again, the collection of this protein domains
align on a string as beads.
And the protein domains are made up of amino acid residue.
So we're talking.
So this is the basic,
so you're saying the protein domain
is the basic building block of the function
that we think about proteins doing.
So, of course, you can always talk about
different building blocks with turtles all the way down.
But there's a point where there is at the point
of the hierarchy where it's the most, the cleanest
element block based on which you can put them together
in different kinds of ways to form complex function.
And you're saying protein domains,
why is that not talked about as often in popular culture?
Well, you know, there are several perspectives on this.
And one, of course, is the historical perspective, right?
So historically, scientists have been able
to structurally resolved to obtain the 3D coordinates
of a protein for, you know, for smaller proteins.
And smaller proteins tend to be a single domain protein.
So we have a protein equal to a protein domain.
And so because of that, the initial suspicion was
that the proteins are, they have globular shapes
and the more of smaller proteins you obtain structurally,
the more you became convinced that that's the case.
And only later when we started having, you know,
alternative approaches.
So, you know, the traditional ones are X-ray crystallography
and NMR spectroscopy.
So these are sort of the two main techniques
that give us the 3D coordinates.
But nowadays, there's huge breakthrough
in cryoelectron microscopy.
So the more advanced methods that allow us to, you know,
to get into the, you know, 3D shapes
of much larger molecules, molecular complexes,
just to give you one of the common examples for this year.
Right?
So the first experimental structure
of a SARS-CoV-2 protein was the cryo-EM structure
of the S protein, so the spike protein.
And so it was solved very quickly.
And the reason for that is the advancement
of this technology is pretty spectacular.
How many domains is the, is it more than one domain?
Oh, yes.
Oh, yes, I mean, so it's a very complex structure.
And we, you know, on top of the complexity
of a single protein, right?
So this structure is actually, is a complex, is a trimer.
So it needs to form a trimer in order to function properly.
What's a complex?
So a complex is a glomeration of multiple proteins.
And so we can have the same protein copied
in multiple, you know, made up in multiple copies
and forming something that we called a Homo oligomer.
Homo means the same, right?
So, so in this case, so the spike protein is the,
is an example of a Homo tetramer, Homo trimer, sorry.
So means three copies of a three copies in order to.
Exactly.
We have these three chains,
the three molecular chains coupled together
and performing the function.
That's what, when you look at this protein from,
from the top, you see a perfect triangle.
So, but other, you know, so other complexes are made up
of, you know, different proteins.
Some of them are completely different.
Some of them are similar, the hemoglobin molecule, right?
So it's actually, it's a protein complex.
It's made of four basic subunits.
Two of them are identical to each other.
Two other are identical to each other,
but they are also similar to each other,
which sort of gives us some ideas about the evolution
of this, you know, of this molecule.
And perhaps one of the hypotheses that, you know,
in the past, it was just a Homo tetramer, right?
So four identical copies, and then it became, you know,
sort of modified, it became mutated over the time
and became more specialized.
Can we linger on the spike protein for a little bit?
Is there something interesting
or like beautifully you find about it?
I mean, first of all, it's an incredibly challenging protein.
And so we, as a part of our sort of research
to understand the structural basis of this virus
to sort of decode, structure decode
every single protein in its proteome,
which, you know, we've been working on the spike protein.
And one of the main challenges was that
cryo-EM data allows us to reconstruct
or to obtain the 3D coordinates
of roughly two-thirds of the protein.
The rest of the one-third of this protein,
it's a part that is buried into the membrane of the virus
and of the viral envelope.
And it also has a lot of unstable structures around it.
So it's chemically interacting somehow
with whatever the heck it's connecting?
Yeah, so people are still trying to understand.
So the nature of, and the role of this one-third.
Because the top part, you know,
the primary function is to get attached to the, you know,
ACE2 receptor, human receptor.
There is also beautiful, you know,
mechanics of how this thing happens, right?
So because there are three different copies
of this chains, you know,
there are three different domains, right?
So we're talking about domains.
So this is the receptor binding domains, RBDs,
that gets untaggled and get ready
to get attached to the receptor.
And now they are not necessarily going in a sync mode.
As a matter of fact.
Say synchronous?
So, yes.
So, and this is where, you know,
another level of complexity comes into play
because right now what we see is,
we typically see just one of the arms going out
and getting ready to be attached to the ACE2 receptors.
However, there was a recent mutation
that people studied in that spike protein.
And a very recently,
a group from UMass Medical School,
we happened to collaborate with groups.
So this is a group of Jeremy Lubin
and a number of other faculty.
They actually solved the mutated structure of the spike
and they showed that actually,
because of these mutations,
you have more than one arms opening up.
And so now, so the frequency of two arms going up
increase quite drastically.
How does that change the dynamics somehow?
It potentially can change the dynamics of,
because now you have two possible opportunities
to get attached to the ACE2 receptor.
It's a very complex molecular process,
mechanistic process.
But the first step of this process
is the attachment of this spike protein,
of the spike trimer to the human ACE2 receptor.
So this is a molecule that sits on the surface
of the human cell.
And that's essentially what triggers
the whole process of encapsulation.
If this was dating, this would be the first date.
So this is the...
In a way, yes.
So is it possible to have the spike protein
just like floating about on its own?
Or does it need that interactability with the membrane?
Yeah, so it needs to be attached,
at least as far as I know.
But when you get this thing attached on the surface,
there is also a lot of dynamics
on how it sits on the surface.
So for example, there was a recent work in,
again, where people use the cryo-electron microscopy
to get the first glimpse of the overall structure.
It's a very low res,
but you still get some interesting details
about the surface, about what is happening inside,
because we have literally no clue
until recent work about how the capsid is organized.
What's the capsid?
So capsid is essentially,
it's the inner core of the viral particle
where there is the RNA of the virus.
And it's protected by another protein and protein
that essentially acts as a shield.
But now we are learning more and more.
So it's actually, it's not just this shield,
it's potentially used for the stability
of the outer shell of the virus.
So it's pretty complicated.
And I mean, understanding all of this is really useful
for trying to figure out like developing a vaccine
or some kind of drug to attack any aspects of this, right?
So I mean, there are many different implications to that.
I mean, first of all, it's important to understand
the virus itself, right?
So in order to understand how it acts,
what is the overall mechanistic process
of this virus replication
of this virus proliferation to the cell, right?
So that's one aspect.
The other aspect is designing new treatments.
And so one of the possible treatments is,
you know, designing nanoparticles.
And so some nanoparticles that will resemble the viral shape
that would have the spike integrated
and essentially would act as a competitor to the real virus
by blocking the ACE2 receptors
and thus preventing the real virus entering the cell.
Now, there are also, you know,
there is a very interesting direction
in looking at the membrane,
at the envelope portion of the protein
and attacking its M protein.
So there are, you know, to give you, you know,
sort of a brief overview,
there are four structural proteins
that these are the proteins that made up
a structure of the virus.
So spike S protein that acts as a trimer.
So it needs three copies.
E envelope protein that acts as a pentamer.
So it needs five copies to act properly.
M is a membrane protein, it forms dimers.
And actually it forms beautiful lattice.
And this is something that we've been studying
and we are seeing it in simulations.
It actually forms a very nice grid
or, you know, threads, you know,
of different dimers attached next to each other.
There's a bunch of copies of each other
and they naturally, when you have a bunch of copies
of each other, they form an interesting lattice.
Exactly.
And, you know, if you think about this, right?
So this complex, you know,
the viral shape needs to be organized somehow,
self-organized somehow, right?
So, you know, if it was a completely random process,
you know, you probably wouldn't have the envelope shell
of the ellipsoid shape.
You know, you would have something, you know,
pre-random, right, shape.
So there is some, you know, regularity
and how this, you know, how this M dimers
get to attach to each other in a very specific,
directed way.
Is that understood at all?
It's not understood.
We are now, we've been working in the past six months
since, you know, we're met.
Actually, this is where we started working
on trying to understand the overall structure
of the envelope and the key components
that made up this, you know, structure.
Wait, does the envelope also have the latest structure
or no?
So the envelope is essentially is the outer shell
of the viral particle.
The N, the nucleocapsid protein,
is something that is inside.
Got it.
But get that.
The N is likely to interact with M.
Does it go M and E?
Like where's the E and N?
So E, those different proteins,
they occur in different copies on the viral particle.
So E, this pentamer complex,
we only have two or three maybe per each particle, okay?
We have 1,000 or so of M dimers
that essentially makes up the entire, you know, outer shell.
So most of the outer shell is the M.
M dimer.
M-protein.
When you say particle, that's the viral on the virus,
the individual virus.
It's a single, yes.
Single element of the virus, single virus.
Single virus, right.
And we have about, you know, roughly 50 to 90 spike trimmers.
Right?
So when you show a-
Per virus particle.
Per virus particle.
So what did you say, 50 to 90?
50 to 90, right?
So this is how this thing is organized.
And so now, typically, right?
So you see these, the antibodies that target spike protein,
you know, spike protein, certain parts of the spike protein,
but there could be some, also some treatments, right?
So these are, you know, these are small molecules
that bind strategic parts of these proteins,
disrupting its function.
So one of the promising directions,
it's one of the newest directions,
is actually targeting the M dimer of the protein.
Targeting the proteins that make up this outer shell.
Because if you're able to destroy the outer shell,
you're essentially destroying the viral particle itself.
So preventing it from, you know, function at all.
So that's, you think is a,
from a sort of cybersecurity perspective,
virus security perspective, that's the best attack vector.
Or like, that's a promising attack vector.
I would say yes.
So I mean, there's still tons of research needs to be,
you know, to be done.
But yes, I think, you know, so.
There's more attack surface, I guess.
More attack surface.
But, you know, from our analysis,
from other evolution analysis,
this protein is evolutionary more stable
compared to the spike protein.
Stable means a more static target.
Well, yeah.
So it doesn't change.
It doesn't evolve from the evolutionary perspective
so drastically as, for example, the spike protein.
There's a bunch of stuff in the news
about mutations of the virus in the United Kingdom.
I also saw in South Africa something.
Maybe that was yesterday.
You just kind of mentioned about stability and so on.
Which aspects of this are mutatable
and which aspects, if mutated, become more dangerous.
And maybe even zooming out
what are your thoughts and knowledge and ideas
about the way it's mutated,
all the news that we've been hearing.
Are you worried about it from a biological perspective?
Are you worried about it from a human perspective?
So I mean, you know, mutations are sort of a general way
for these viruses to evolve, right?
So it's, you know, it's essentially,
this is the way they evolve.
This is the way they were able to jump
from one species to another.
We also see, you know, some recent jumps.
There were some incidents of this virus jumping
from human to dogs.
So, you know, there is some danger in those jumps
because, you know, every time it jumps, it also mutates, right?
So when it jumps to the species and jumps back, right?
So it acquires some mutations that are sort of driven
by the environment of a new host, right?
And it's different from the human environment.
And so we don't know whether the mutations
that are acquired in the new species are neutral
with respect to the human host or maybe, you know,
maybe damaging.
Yeah, change is always scary.
But so are you worried about, I mean,
it seems like because the spread is during winter,
now it seems to be exceptionally high.
And especially with a vaccine just around the corner,
already being actually deployed,
there's some worry that this puts evolutionary pressure,
selective pressure on the virus.
And for it to mutate, is that a source of worry?
Well, I mean, there is always this thought, you know,
in the scientist's mind, you know, what will happen, right?
So I know there have been discussions about
sort of the arms race between the, you know,
the ability of the humanity to, you know, to get vaccinated faster,
then the virus, you know, essentially, you know,
becomes, you know, resistant to the vaccine.
I mean, I don't worry that much,
simply because, you know, there is not that much evidence to that.
To aggressive mutation around the vaccine.
Exactly, you know, obviously, there are mutations around the vaccine.
So the reason we get vaccinated every year
against the season of the mutations, right?
But, you know, I think it's important to study it.
No doubts, right?
So I think one of the, you know, to me, again, I might be biased
because, you know, we've been trying to do that as well.
So, but one of the critical directions in understanding the virus
is to understand its evolution in order to sort of understand
the mechanisms, the key mechanisms that lead the virus to jump,
you know, the Nordic viruses to jump from species,
from species to another, that the mechanisms that lead the virus
to become resistant to vaccines, also to treatments, right?
And hopefully, that knowledge will enable us to sort of forecast
the evolutionary traces, the future evolutionary traces of this virus.
I mean, what from a biological perspective,
this might be a dumb question, but is there parts of the virus
that if souped up, like through mutation,
could make it more effective at doing its job?
We're talking about this specific coronavirus, like,
because we were talking about the different, like the membrane,
the M protein, the E protein, the N and the S, the spike.
Is there some part?
And there are 20 or so more in addition to that.
But is that a dumb way to look at it?
Like, which of these, if mutated, could have the greatest impact,
potentially damaging impact on the effectiveness of the virus?
So, it's actually, it's a very good question,
because, and the short answer is, we don't know yet.
But, of course, there is capacity of this virus to become more efficient.
The reason for that is, you know, so if you look at the virus,
I mean, it's a machine, right?
So, it's a machine that does a lot of different functions.
And many of these functions are sort of nearly perfect,
but they are not perfect.
And those mutations can make those functions more perfect.
For example, the attachment to ACE2 receptor, right, of the spike, right?
So, you know, is it, has this virus reached the efficiency
in which the attachment is carried out?
Or there are some mutations that still to be discovered, right,
that will make this attachment sort of stronger,
or, you know, something more, in a way, more efficient
from the point of view of this virus functioning.
That's sort of the obvious example.
But if you look at each of these proteins,
I mean, it's there for a reason.
It performs certain function.
And it could be that certain mutations will, you know, enhance this function.
It could be that some mutations will make this function much less efficient.
So, that's also the case.
Since we're talking about the evolutionary history of a virus,
let's zoom back out and look at the evolutionary proteins.
I would glance at this 2010 Nature paper on the quote,
ongoing expansion of the protein universe.
And then, you know, it kind of implies and talks about that proteins started
with a common ancestor, which is, you know, kind of interesting.
It's interesting to think about, like, even just, like, the first organic thing
that started life on Earth.
And from that, there's now, you know, what is it, 3.5 billion years later,
there's now millions of proteins.
And they're still evolving.
And that's, you know, in part one of the things that you're researching.
Is there something interesting to you about the evolution of proteins
from this initial ancestor to today?
Is there something beautiful and insightful about this long story?
So, I think, you know, if I were to pick a single keyword about protein evolution,
I would pick modularity, something that we talked about in the beginning.
And that's the fact that the proteins are no longer considered as, you know,
as a sequence of letters.
There are hierarchical complexities in the way these proteins are organized.
And these complexities are actually going beyond the protein sequence.
It's actually going all the way back to the gene, to the nucleotide sequence.
And so, you know, again, these protein domains, they are not only functional building blocks.
They are also evolutionary building blocks.
And so, what we see in the sort of, in the later stages of evolution,
I mean, once these stable, structurally and functionally building blocks were discovered,
they essentially, they stay, those domains stay as such.
So, that's why if you start comparing different proteins,
you will see that many of them will have similar fragments.
And those fragments will correspond to something that we call protein domain families.
And so, they are still different because you still have mutations and, you know,
the, you know, different mutations are attributed to, you know,
diversification of the function of this, you know, protein domain.
However, you don't, you very rarely see, you know,
the evolutionary events that would split this domain into fragments.
Because, and it's, you know, once you have the domain split,
you actually, you know, you can completely cancel out its function
or at the very least, you can reduce it.
And that's not, you know, efficient from the point of view of the, you know, of the cell function.
So, the protein domain level is a very important one.
Now, on top of that, right, so if you look at the proteins, right,
so you have these structural units and they carry out the function.
But then, much less is known about things that connect these protein domains.
Something that we call linkers.
And those linkers are completely flexible, you know, parts of the protein
that nevertheless carry out a lot of function.
It's like little tails, little heads.
So, we do have tails, so they call termini, C and N termini.
So, these are things right on the, on one and another ends of the protein sequence.
So, they are also very important, so they attribute it to very specific interactions between the proteins.
But you're referring to the links between domains?
That connect the domains.
And, you know, apart from the, just the simple perspective,
if you have, you know, a very short domain, you have, sorry, a very short linker,
you have two domains next to each other.
They are forced to be next to each other.
If you have a very long one, you have the domains that are extremely flexible
and they carry out a lot of sort of spatial reorganization, right?
That's awesome.
But on top of that, right, just this linker itself, because it's so flexible,
it actually can adapt to a lot of different shapes.
And therefore, it's a very good interactor when it comes to interaction
between this protein and other protein.
So, these things also evolve, you know, and they, in a way,
have different sort of laws of, or the driving laws that underlie the evolution
because they no longer need to preserve certain structure, right,
unlike protein domains.
And so, on top of that, you have something that is even less studied.
And this is something that attributed to the concept of alternative splicing.
So, alternative splicing.
So, it's a very cool concept.
It's something that we've been fascinated about for, you know, over a decade in my lab
and trying to do research with that.
But so, you know, so typically, you know, a simplistic perspective
is that one gene is equal one protein product, right?
So, you have a gene, you know, you transcribe it and translate it,
and it becomes a protein.
In reality, when we talk about eukaryotes, especially sort of more recent eukaryotes
that are very complex, the gene is no longer equal to one protein.
It actually can produce multiple functionally, you know, active protein products.
And each of them is, you know, is called an alternatively spliced product.
The reason it happens is that if you look at the gene, it actually has, it has also blocks.
And the blocks, some of which, and it essentially, it goes like this.
So, we have a block that will later be translated, we call it exon.
Then we'll have a block that is not translated, cut out.
We call it intron.
So, we have exon, intron, exon, intron, et cetera, et cetera, et cetera, right?
And sometimes you can have, you know, dozens of these exons and introns.
So, what happens is during the process when the gene is converted to RNA,
we have things that are cut out, the introns that cut out,
and exons that now get assembled together.
And sometimes we will throw out some of the exons.
And the remaining protein product will become different, right?
So, now you have fragments of the protein that no longer there.
They were cut out with the introns.
Sometimes you will essentially take one exon and replace it with another one, right?
So, there's some flexibility in this process.
So, that creates a whole new level of complexity.
Is this random though?
It's not random. We, and this is where I think now the appearance
of this modern single cell and before that tissue level sequencing,
next generation sequencing techniques such as RNA-Seq,
allows us to see that these are the events that often happen in response,
it's a dynamic event that happens in response to disease
or in response to certain developmental stage of a cell.
And this is an incredibly complex layer that also undergoes,
I mean, because it's at the gene level, right?
So, it undergoes certain evolution, right?
And now we have this interplay between what is happening in the protein world
and what is happening in the gene and RNA world.
And for example, it's often that we see that the boundaries of these exons
coincide with the boundaries of the protein domains, right?
So, there is close interplay to that.
It's not always, I mean, otherwise it would be too simple, right?
But we do see the connection between those sort of machineries.
And obviously the evolution will pick up this complexity and, you know,
select for whatever is successful.
Yeah, we see that complexity in play
and makes this question, you know, more complex but more exciting.
A small detour, I don't know if you think about this into the world of computer science.
There's a Douglas Haasdatter, I think, came up with a name of Quine,
which are, I don't know if you're familiar with these things,
but it's computer programs that have, I guess, exon and intron,
and they copy, the whole purpose of the program is to copy itself.
So, it prints copies of itself, but can also carry information inside of it.
So, it's a very kind of crude, fun exercise of,
can we sort of replicate these ideas from cells?
Can we have a computer program that when you run it, just print itself,
the entirety of itself, and does it in different programming languages and so on.
I've been playing around and writing them.
It's a kind of fun little exercise.
You know, when I was a kid, so, you know, it was essentially one of the sort of main stages
in Informatics Olympics that you have to reach in order to be any so good,
is you should be able to write a program that replicates itself.
And so, the tax then becomes even, you know, sort of more complicated.
So, what is the shortest program?
And of course, it's a function of a programming language,
but yeah, I remember, you know, long, long, long time ago when we tried to, you know,
to make it short and short and find the shortcuts.
There's actually a stack exchange.
There's an entire site called CodeGolf, I think, where the entirety is just a competition.
People just come up with whatever task.
I don't know, like a write code that reports the weather today.
And the competition is about whatever programming language,
what is the shortest program, and it makes you actually, people should check it out
because it makes you realize there's some weird programming languages out there.
But, you know, just to dig on that a little deeper, do you think, you know,
in computer science, you don't often think about programs.
There's like the machine learning world now that's still kind of basic programs.
And then there's humans that replicate themselves, right?
And there's these mutations and so on.
Do you think we'll ever have a world where there's programs that kind of have an evolutionary process?
So, I'm not talking about evolutionary algorithms,
but I'm talking about programs that kind of mate with each other and evolve
and, like, on their own, replicate themselves.
So, this is kind of the idea here is, you know, that's how you can have a runaway thing.
So, we think about machine learning as a system that gets smarter and smarter and smarter and smarter.
At least the machine learning systems of today are, like, it's a program that you can, like, turn off
as opposed to throwing a bunch of little programs out there and letting them, like, multiply and mate and evolve and replicate.
Do you ever think about that kind of world, you know, when we jump from the biological systems
that you're looking at to artificial ones?
I mean, it's almost like you take the sort of the area of intelligent agents, right?
Which are essentially the independent sort of codes that run and interact and exchange the information, right?
So, I don't see why not.
I mean, I, you know, it could be sort of a natural evolution in this area of computer science.
I think it's kind of an interesting possibility.
It's terrifying, too, but I think it's a really powerful tool.
Like, to have, like, agents that interact, you know, we have social networks with millions of people and they interact.
I think it's interesting to inject into that.
It was already injected into that bot, right?
But those bots are pretty dumb, you know, they're probably pretty dumb algorithms.
You know, it's interesting to think that there might be bots that evolve together with humans.
And there's the sea of humans and robots that are operating first in the digital space.
And you can also think, I love the idea, some people worked, I think at Harvard, at Penn, there's robotics labs that, you know,
take as a fundamental task to build a robot that, given extra resources, can build another copy of itself.
Like in the physical space, which is super difficult to do, but super interesting.
I remember there's like research on robots that can build a bridge.
So they make a copy of themselves and they connect themselves.
So it's like self-building bridge based on building blocks.
You can imagine like a building that self-assembles.
So it's basically self-assembling structures from robotic parts.
But it's interesting to, within that robot, add the ability to mutate and do all the interesting, like, little things that you're referring to in evolution
to go from a single origin protein building block to like this weird complexity.
And if you think about this, I mean, you know, the bits and pieces are there, you know.
So you mentioned the evolutionary algorithm, right?
You know, so this is sort of, and maybe sort of the goal is in a way different, right?
So the goal is to, you know, to essentially to optimize your search, right?
So, but sort of the ideas are there.
So people recognize that, you know, that the, you know, recombination events lead to global changes in the search trajectories.
The mutations event is a more refined, you know, step in the search.
Then you have, you know, other sort of nature-inspired algorithm, right?
So one of the reasons that, you know, I think it's one of the funnest one is the slime-based algorithm, right?
So I think the first was introduced by the Japanese group where it was able to solve some pre-complex problems.
So that's, you know, and then I think there are still a lot of things we've yet to, you know, borrow from the nature, right?
So there are a lot of sort of ideas that nature, you know, gets to offer us that, you know, it's up to us to grab it and to, you know, get the best use of it.
Including neural networks, you know, we have a very crude inspiration from nature on neural networks.
Maybe there's other inspirations to be discovered in the brain or other aspects of the various systems, even like the immune system, the way it interplays.
I recently started to understand that the immune system has something to do with the way the brain operates.
There's multiple things going on in there, all of which are not modeled in artificial neural networks.
And maybe if you throw a little bit of that biological spice in there, you'll come up with something cool.
I'm not sure if you're familiar with the Drake equation.
I just did a video on it yesterday because I wanted to give my own estimate of it.
It's an equation that combines a bunch of factors to estimate how many alien civilizations.
Oh yeah, I've heard about it.
So one of the interesting parameters, you know, it's like how many stars are born every year, how many planets are on average per star, how many habitable planets are there.
And then the one that starts being really interesting is the probability that life emerges on a habitable planet.
So like, I don't know if you think about, you certainly think a lot about evolution,
but do you think about the thing which evolution doesn't describe, which is like the beginning of evolution, the origin of life.
I think I put the probability of life developing a habitable planet at 1%.
This is very scientifically rigorous.
Okay, well, first, at a high level for the Drake equation, what would you put that percent that on Earth?
And in general, do you have something, do you have thoughts about how life might have started?
You know, like the proteins being the first kind of one of the early jumping points?
Yes, so I think back in 2018, there was a very exciting paper published in Nature where they found one of the simplest amino acids, glycine.
In a comet dust.
So this is, I apologize if I don't pronounce, it's a Russian named comet.
I think Chugryumov-Gerasimenko.
This is the comet where, and there was this mission to get close to this comet and get the stardust from its tail.
And when scientists analyzed it, they actually found traces of glycine, which makes up one of the 20 basic amino acids that makes up proteins.
So that was kind of very exciting, right?
But the question is very interesting, right? So if there is some alien life, is it going to be made of proteins, right?
Or maybe RNAs, right?
So we see that the RNA viruses are certainly very well-established sort of group of molecular machines, right?
So yes, it's a very interesting question.
What probability would you put? How unlikely just on earth do you think this whole thing is that we got going?
Are we really lucky or is it inevitable? What's your sense when you sit back and think about life on earth?
Is it higher or lower than 1%?
Well, because 1% is pretty low, but it's still like, damn, that's a pretty good chance.
Yes, it's a pretty good chance. I mean, I would personally, but again, you know, I'm probably not the best person to do such estimations.
But intuitively, I would probably put it lower. But still, I mean, you know...
So we're really lucky here on earth.
Or the conditions are really good.
I think that everything was right in a way, right?
So still, the conditions were not ideal if you try to look at what was several billions years ago when the life emerged.
So there is something called the rare earth hypothesis that, you know, in counter to the Drake equation says that the, you know, the conditions of earth, if you actually were to describe earth, it's quite a special place.
So special, it might be unique in our galaxy and potentially, you know, close to unique in the entire universe.
Like it's very difficult to reconstruct those same conditions. And what the rare earth hypothesis argues is all those different conditions are essential for life.
And so that's sort of the counter, you know, like all the things we...
Thinking that earth is pretty average. I mean, I can't really... I'm trying to remember to go through all of them, but just the fact that it is shielded from a lot of asteroids, obviously the distance to the sun,
but also the fact that it's like a perfect balance between the amount of water and land and all those kinds of things.
I don't know. There's a bunch of different factors that I don't remember. There's a long list, but it's fascinating to think about if in order for something like proteins and DNA and RNA to emerge, you need...
And basic living organisms, you need to be a very close and earth-like planet, which would be sad or exciting. I don't know.
If you ask me, in a way, I put a parallel between our own research and... I mean, from the intuitive perspective, you have those two extremes.
And the reality is never very rarely falls into the extremes. It's always the optimums always reached somewhere in between.
And that's what I tend to think. I think that we're probably somewhere in between, so they were not unique, unique, but again, the chances are reasonably small.
The problem is we don't know the other extremes. I tend to think that we don't actually understand the basic mechanisms of what this is all originated from.
It seems like we think of life as this distinct thing, maybe intelligence as a distinct thing, maybe the physics from which planets and suns are born as a distinct thing.
But that could be a very... It's like the Stephen Wolfram thing. It's like the... From simple rules emerges greater and greater complexity.
So I tend to believe that just life finds a way. We don't know the extreme of how common life is, because it could be life is like everywhere.
So everywhere that it's almost laughable, that we're such idiots to think... It's ridiculous to even think... It's like ants thinking that their little colony is the unique thing and everything else doesn't exist.
I mean, it's also very possible that that's the extreme, and we're just not able to maybe comprehend the nature of that life.
Just to stick on alien life for just a brief moment more, there is some signs of life on Venus in gaseous form.
There's hope for life on Mars, probably extinct. We're not talking about intelligent life, although that has been in the news recently.
We're talking about basic bacteria.
And then also, I guess, there's a couple moons that I guess... Europe. Yeah, Europa, which is Jupiter's moon. I think there's another one. Are you... Is that exciting? Is it terrifying to you that we might find life? Do you hope we find life?
I certainly do hope that we find life. I mean, it was very exciting to hear about this news about the possible life on Venus.
It's been nice to have hard evidence of something, which is what the hope is for Mars and Europa. But do you think those organisms would be similar biologically, or would they even be sort of carbon-based if we do find them?
I would say they would be carbon-based. How similar? It's a big question, right? The moment we discover things outside Earth, right? Even if it's a tiny little single cell, I mean, there is so much.
Just imagine that. That would be so...
I think that would be another turning point for the science.
And especially if it's different in some very new way, that's exciting because that says... That's a definitive state, not a definitive, but a pretty strong statement that life is everywhere in the universe.
To me, at least, that's really exciting. You brought up Joshua Letterberg in an offline conversation. I think I'd love to talk to you about AlphaFold, and this might be an interesting way to enter that conversation because...
So he won the 1958 Nobel Prize in Physiology and Medicine for discovering that bacteria can mate and exchange genes, but he also did a ton of other stuff, like we mentioned, helping NASA find life on Mars and the...
Dendrol.
Dendrol, the chemical expert system. Expert systems. Remember those?
Do you... What do you find interesting about this guy and his ideas about artificial intelligence in general?
I have a kind of personal story to share. So I started my PhD in Canada back in 2000.
And so essentially my PhD was... So we were developing a new language for symbolic machine learning. So it's different from the feature-based machine learning. And one of the sort of cleanest applications of this approach, of this formalism, was two cheminformatics and computer-aided drug design.
So essentially, as a part of my research, I developed a system that essentially looked at chemical compounds of, say, the same therapeutic category, male hormones, and tried to figure out the structural fragments that are the structural building blocks that are important,
that define this class versus structural building blocks that are there just to complete the structure. But they are not essentially the ones that make up the key chemical properties of this therapeutic category.
And for me it was something new. I was trained as an applied mathematician with some machine learning background, but computer-aided drug design was completely new territory.
So because of that, I often find myself asking lots of questions on one of these sort of central forums. Back then there were no Facebooks or stuff like that.
What's a forum?
It's a forum. It's essentially like a bulletin board.
On the internet.
Yeah, so essentially you have a bunch of people and you post a question and you get an answer from different people. And back then, one of the most popular forums was CCL.
I think computational chemistry, not library, but something like that. But CCL, that was the forum. And there I asked a lot of dumb questions.
Yes, I asked questions. I also shared some information about our formalism, how we do, and whether whatever we do makes sense.
And I remember that one of these posts, I still remember, I would call it desperately looking for a chemist advice, something like that.
And so I asked my question, I explained how our formalism is, what it does, and what kind of applications I'm planning to do. And it was in the middle of the night and I went back to bed.
And next morning, I have a phone call from my advisor who also looked at this forum. It's like, you won't believe who replied to you.
And it's like, who? And he said, well, you know, there is a message to you from Joshua Lederberg. And my reaction was like, who is Joshua Lederberg?
Your advisor hung up. So essentially, Joshua wrote me that we had conceptually similar ideas in the Dendral project. You may want to look it up.
And we should also, sorry, and it's a side comment, say that even though he won the Nobel Prize at a really young age, in 58.
He was, I think, he was what, 33. Yeah, it's just crazy. So anyway, hence in the 90s, responding to young whippersnappers on the CCL forum.
And so back then, he was already very senior. I mean, he unfortunately passed away back in 2008. But, you know, back in 2001, he was, I mean, he was a professor emeritus at Rockefeller University.
And that was actually, believe it or not, one of the reasons I decided to join as a postdoc, the group of Andrei Saleh, who was at Rockefeller University, with the hope that I could actually have a chance to meet Joshua in person.
And I met him very briefly, right? Just because he was walking, you know, there's a little bridge that connects the sort of the research campus with the sort of Skype scrappers that Rockefeller owns.
There were, you know, postdocs and faculty and graduate students live. And so I met him, you know, and I had a very short conversation, you know. But so I started, you know, reading about Dendral.
And I was amazed, you know, it's, we're talking about 1960, right? The ideas were so profound.
Well, what's the fundamental idea of it? The reason to make this is even crazier. So, so, so Lederberg wanted to make a system that would help him study the extraterrestrial molecules, right?
So, so the idea was that, you know, the way you study the extraterrestrial molecules is you do the mass spec analysis, right? And so the mass spec gives you sort of bits, numbers about essentially gives you the ideas about the possible fragments, or, you know, atoms,
you know, and maybe a little fragments, pieces of this molecule that make up the molecule, right? So now you need to sort of to decompose this information and to figure out what was the whole before, you know, became fragments, bits and pieces, right?
So, so in order to make this, you know, to have this tool, the idea of Lederberg was to connect chemistry, computer science, and to design this so-called expert system that looks, that takes into account, that takes as an input the mass spec data,
the possible database of possible molecules, and essentially try to sort of induce the molecule that would correspond to this spectrum, or, you know, essentially what this project ended up being was that, you know, it would provide a list of
candidates that then a chemist would look at and make final decision. So, but the original idea as opposed to solve the entirety of this problem automatically.
Yes. So, so, so he, you know, so, so he, back then, he approached, yes, believe that. It's amazing. I mean, still blows my mind, you know, that it's, that's, and this was essentially the origin of the modern bioinformatics, cheminformatics, back in the 60s.
Yeah. So that's, that's, you know, so every time you deal with projects like this, with the, you know, research like this, you just, you know, so the power of the, you know, intelligence of these people is just, you know, overwhelming.
Do you think about expert systems? Is there, and why they kind of didn't become successful, especially in the space of bioinformatics, where it does seem like there's a lot of expertise in humans.
And, you know, it's, it's possible to see that a system like this could be made very useful.
Right. So it's, it's actually, it's a great question. And this is something so, you know, so, you know, at my university, I teach artificial intelligence. And, you know, we start the my first two lectures are on the history of AI.
And there we, you know, we try to, you know, go through the main stages of AI. And so, you know, the question of why expert systems failed or became obsolete.
It's actually a very interesting one. And there are, you know, if you try to read the, you know, the historical perspectives, there are actually two lines of thoughts.
One is that they, they were essentially not up to the expectations. And so therefore they were replaced, you know, by, by other things. Right.
The other one was that completely opposite one, that they were too good. And, and as a result, they essentially became sort of a household name. And then essentially they got transformed.
I mean, they, in both cases, sort of the outcome was the same, they evolved into something.
Yeah.
Right. And that's what I, you know, if, if I look at this, right, so the modern machine learning.
So there's echoes in the modern machine learning.
I think so. I think so. Because, you know, if you, if you think about this, you know, and how we design, you know, the most successful algorithms, including Alpha fold, right, you built in the knowledge about the domain that you study.
Right. So, so you built in your expertise.
So speaking of Alpha fold, the DeepMinds Alpha fold two recently was announced to have, quote unquote, solved protein folding.
How exciting is this to you? It seems to be one of the, one of the exciting things that have happened in 2020. It's incredible accomplishment from the looks of it.
What part of it is amazing to you? What part would you say is overhyped or maybe misunderstood?
It's definitely a very exciting achievement to give you a little bit of perspective, right? So, so in bioinformatics, we have several competitions.
And so the way, you know, you often hear how those competitions have been explained to sort of to non bioinformaticians is that, you know, they call it bioinformatics Olympic games.
And there are several disciplines, right? So, so the, the, the historically one of the first one was the discipline in predicting the protein structure, predicting the 3D coordinates of the protein.
But there are some others. So the predicting protein functions, predicting effects of mutations on protein functions, then predicting a protein, protein interactions.
So, so the original one was CASP or critical assessment of, of protein structure.
And the, you know, typically what happens during these competitions is, you know, scientists, experimental scientists solve the, the structures, but don't put them into the protein data bank, which is the centralized database.
That contains all the 3D coordinates. Instead, they hold it and release protein sequences.
And now the challenge of the community is to predict the 3D structures of these proteins and then use the experimentary solve structures to assess which one is the closest one, right?
And this competition, by the way, just a bunch of different tangents. And maybe you can also say what is protein folding. And this competition CASP competition is, has become the gold standard.
And that's what was used to say that protein folding was solved. So I just added a little, yeah, just a bunch.
So if you can, whenever you say stuff, maybe throw in some of the basics for the folks that might be outside of the field. Anyway, sorry.
So, so, yeah, so, you know, so the reason it's, it's, you know, it's relevant to our understanding of protein folding is because, you know, we, we've yet to learn how the folding mechanistically works, right?
So there are different hypotheses. What happens to this fold? For example, there is a hypothesis that the folding happens by, you know, also in the modular fashion, right?
So that, you know, we have protein domains that get folded independently because the structure is stable and then the whole protein structure gets formed.
But, you know, within those domains, we also have so-called secondary structure, the small alpha helices, beta sheets.
So these are, you know, elements that are structurally stable. And so, and the question is, you know, when they, when do they get formed?
Because some of the secondary structure elements, you have to have, you know, a fragment in the beginning and say the fragment in the middle, right?
So, so you cannot potentially start having the full fold from the get go, right?
So, so it's still, you know, it's still a big enigma. What, what happens?
We know that it's an extremely efficient and stable process, right?
So there's this long sequence and the fold happens really quickly.
Exactly.
So that's really weird, right?
And it happens like the same way almost every time.
Exactly. Exactly.
That's really weird.
That's freaking weird.
That's why it's such an amazing thing.
But most importantly, right?
So it's, you know, so when you see the, you know, the translation process, right?
So when you don't have the whole protein translated, right?
It's still being translated, you know, getting out from the ribosome, you already see some structural, you know, fragmentation.
So, so folding starts happening before the whole protein gets produced, right?
And so this is, this is obviously, you know, one of the biggest questions in, you know, in modern molecular biologies.
Not, not like maybe what happens?
Like that's not as bigger than the question of folding.
That's the question of like, like deeper fundamental idea of folding.
Yes.
Behind folding.
Exactly.
So, you know, so obviously if we are able to predict the end product of protein folding,
we are one step closer to understanding sort of the mechanisms of the protein folding,
because we can then potentially look and start probing what are the critical parts of this process
and what are not so critical parts of this process.
So now we can start decomposing this, you know, so, so, so in the way this protein structure prediction algorithm can be,
can be used as a tool, right?
So, so you change the, you know, you modify the protein, you get back to this tool, it predicts.
Okay, it's completely, it's completely unstable.
Yeah, which, which aspects of the input will have a big impact on the output?
Exactly.
Exactly.
So, so what happens is, you know, we typically have some sort of incremental advancement.
You know, each stage of this CASP competition, you have groups with incremental advancement.
And, you know, historically, the top performing groups were, you know, they were not using machine learning.
They were using very advanced biophysics, combined with bioinformatics, combined with, you know, the data mining.
And that was, you know, that would enable them to obtain protein structures of those proteins that don't have any structural results relatives.
Because, you know, if we have another protein, say the same protein, but coming from a different species,
we could potentially derive some ideas, and that's so-called homology or comparative modeling,
where we'll derive some ideas from the previously known structures.
And that would help us tremendously in, you know, in reconstructing the 3D structure overall.
But what happens when we don't have these relatives?
This is when it becomes really, really hard, right?
So, that's so-called de novo, you know, de novo protein structure prediction.
And in this case, those methods were traditionally very good.
But what happened in the last year, the original alpha fold came into,
and over sudden, it's much better than everyone else.
This is 2018.
Oh, the competition is only every two years, I think.
And then, so, you know, it was sort of kind of of a shockwave to the bioinformatics community
that, you know, we have like a state-of-the-art machine learning system that does, you know, structure prediction.
And essentially what it does, you know, so, you know, if you look at this,
it actually predicts the context.
So, you know, so, the process of reconstructing the 3D structure
starts by predicting the context between the different parts of the protein.
And the context essentially is the parts of the proteins that are in a close proximity to each other.
Right, so actually the machine learning part seems to be estimating,
you can correct me if I'm wrong here, but it seems to be estimating the distance matrix,
which is like the distance between the different parts.
Yeah, so we call the contact map.
Contact map.
Right, so once you have the contact map, the reconstruction is becoming more straightforward.
Right, but so the contact map is the key.
And so, you know, so that's what happened, and now we started seeing in this current stage, right,
in the most recent one, we started seeing the emergence of these ideas in other people's works.
Right, but yet here's, you know, AlphaFold 2 that again outperforms everyone else.
And also by introducing yet another wave of the machine learning ideas.
Yeah, there doesn't seem to be also an incorporation.
First of all, the paper is not out yet, but there's a bunch of ideas already out.
There does seem to be an incorporation of this other thing, I don't know if it's something that you could speak to,
which is like the incorporation of like other structures, like evolutionary similar structures
that are used to kind of give you hints.
Yes, so evolutionary similarity is something that we can detect at different levels.
Right, so we know, for example, that the structure of proteins is more conserved than the sequence.
The sequence could be very different, but the structural shape is actually still very conserved.
So that's sort of the intrinsic property that, you know, in a way related to protein folds,
you know, to the evolution of the, you know, of the protein of proteins and protein domains, etc.
But we know that, I mean, we've been multiple studies.
And, you know, ideally if you have structures, you know, you should use that information.
However, sometimes we don't have this information.
Instead, we have a bunch of sequences, sequences we have a lot.
Right, so we have, you know, hundreds, thousands of, you know, different organisms sequence.
Right, and by taking the same protein, but in different organisms and aligning it,
so making it, you know, making the corresponding positions aligned,
we can actually say a lot about sort of what is conserved in this protein,
and therefore, you know, structure is more stable, what is diverse in this protein.
So on top of that, we could provide sort of the information about the secondary structure of this protein, etc.
So this information is extremely useful, and it's already there.
So while it's tempting to, you know, to do a complete ab initio, so you just have a protein sequence and nothing else,
the reality is such that we are overwhelmed with this data.
So why not use it?
And so, yeah, so I'm looking forward to reading this paper.
It does seem to, like they've, in the previous version of Alpha Fold, they didn't, for this evolutionary similarity thing, they didn't use machine learning for that.
Or they, rather, they used it as like the input to the entirety of the neural net, like the features, derived from the similarity.
It seems like there's some kind of quote, unquote, iterative thing where it seems to be part of the learning process is the incorporation of this evolutionary similarity.
Yeah, I don't think there is a bio archive paper, right?
There's nothing.
There's a blog post that's written by a marketing team, essentially.
Yeah.
You know, it has some scientific similarity, probably, to the actual methodology used, but it could be, it's like interpreting scripture.
It could be just poetic interpretations of the actual work, as opposed to direct connection to the work.
So now, speaking about protein folding, right?
So, you know, in order to answer the question whether or not we have solved this, right?
So we need to go back to the beginning of our conversation.
You know, with the realization that, you know, an average protein is that typically what the cusp has been focusing on is the, you know, this competition has been focusing on the single, maybe two-domain proteins that are still very compact.
And even those ones are extremely challenging to solve, right?
But now we talk about, you know, an average protein that has two, three protein domains.
If you look at the proteins that are in charge of the, you know, of the process with the neural system, right?
Perhaps one of the most recently evolved sort of systems in the organism, right?
All of them, well, the majority of them are highly multi-domain proteins.
So they are, you know, some of them have five, six, seven, you know, and more domains, right?
And, you know, we are very far away from understanding how these proteins are folded.
So the complexity of the protein matters here, the complexity of the protein modules or the protein domains.
So you're saying solved, so the definition of solved here is particularly the cast competition achieving human level,
not human level, achieving experimental level performance on these particular sets of proteins that have been used in these competitions.
Well, I mean, you know, I do think that, you know, especially with regards to the alpha fold, you know,
it is able to, you know, to solve, you know, at the near experimental level,
a pretty big majority of the more compact proteins, like, or protein domains,
because again, in order to understand how the overall protein, you know, multi-domain protein fold,
we do need to understand the structure of its individual domains.
I mean, unlike if you look at alpha zero or like mu zero, if you look at that work, you know, it's nice,
reinforcement learning, self-playing mechanisms are nice because it's all in simulation,
so you can learn from just huge amounts, like you don't need data.
The problem with proteins, like the size, I forget how many 3D structures have been mapped,
but the training data is very small, no matter what.
It's like millions, maybe a one or two million or something like that.
But it's some very small number, but like, it doesn't seem like that's scalable.
There has to be, I don't know, it feels like you want to somehow 10x the data or 100x the data somehow.
Yes, but we also can take advantage of homology models, right?
So the models that are of very good quality because they are essentially obtained based on the evolutionary information.
So there is a potential to enhance this information and use it again to empower the training set.
I think it's been one of these sort of churning events where you have a system that is a machine learning system
that is truly better than the more conventional biophysics-based methods.
That's a huge leap.
This is one of those fun questions, but where would you put it in the ranking of the greatest breakthroughs in artificial intelligence history?
So like, okay, so let's see who's in the running.
Maybe you can correct me.
So you got like AlphaZero and AlphaGo beating the world champion at the game of Go.
Thought to be impossible like 20 years ago, or at least the AI community was highly skeptical.
Then you got like also DBlue original Kasparov.
You have deep learning itself like the, maybe what would you say, the AlexNet ImageNet moment.
So the first network achieving human level performance, super not, that's not true, achieving like a big leap in performance on the computer vision problem.
There is OpenAI, the whole like GPT-3, that whole space of transformers and language models just achieving this incredible performance of application of neural networks to language models.
Boston Dynamics pretty cool, like robotics.
People are like, there's no AI, no, no, there's no machine learning currently, but AI is much bigger than machine learning.
So that just the engineering aspect, I would say is one of the greatest accomplishments in engineering side.
Engineering meaning like mechanical engineering of robotics ever.
Then of course autonomous vehicles, you can argue for Waymo, which is like the Google self-driving car, or you can argue for Tesla, which is like actually being used by hundreds of thousands of people on the road today in machine learning system.
And I don't know if you can, what else is there?
But I think that's it.
And then Alpha4, many people are saying up there, potentially number one, would you put them at number one?
Well, in terms of the impact on the science and on the society beyond, it's definitely, to me, would be one of the top three.
Maybe, I mean, I'm probably not the best person to answer that.
But I do have, I remember my, back in, I think, 1997, when Deep Blue, that Kasparov, it was, I mean, it was a shock.
I mean, it was, and I think for the, you know, for the, you know, pre-substantial part of the world, that especially people who have some, you know, some experience with chess, right?
And realizing how incredibly human this game, how, you know, how much of a brain power you need, you know, to reach those, you know, those levels of grandmasters, right?
And it's probably one of the first time, and how good Kasparov was.
And again, yeah, so Kasparov is actually one of the best ever, right?
And you get a machine that beats him, right?
So it's the first time a machine probably beat a human at that scale of a thing, of anything.
Yes.
Yes.
So that was, to me, that was like, you know, one of the groundbreaking events in the history of ayah.
Yeah, that's probably number one.
That's probably, like, we don't, it's hard to remember.
It's like Muhammad Ali versus, I don't know, any other Mike Tyson, something like that.
It's like, nah, you got to put Muhammad Ali at number one.
Same with Dblue, even though it's not machine learning based.
Still, it uses advanced search, and search is the integral part of ayah, right?
People don't think of it that way at this moment.
In Vogue currently, search is not seen as a fundamental aspect of intelligence,
but it very well, and you very likely is.
In fact, I mean, that's what neural networks are.
There's just performing search on the space of parameters.
And it's all search.
All of intelligence is some form of search,
and you just have to become clever and clever at that search problem.
And I also have another one that you didn't mention.
That's one of my favorite ones.
So you probably heard of this.
It's, I think it's called Deep Rembrandt.
It's the project where they trained.
I think there was a collaboration between the experts in Rembrandt painting in Netherlands,
and a group, an artificial intelligence group,
where they train an algorithm to replicate the style of the Rembrandt,
and they actually printed a portrait that never existed before in the style of Rembrandt.
I think they printed it on the canvas,
using pretty much the same types of paints,
and to me it was mind-blowing.
And the space of art, that's interesting.
There hasn't been, maybe that's it,
but I think there hasn't been an image in that moment yet in the space of art.
You haven't been able to achieve superhuman level performance in the space of art,
even though there was a big famous thing where there was a piece of art was purchased,
I guess, for a lot of money.
Yes.
Yeah.
But it's still, you know, people are like in space of music at least.
That's, you know, it's clear that human created pieces are much more popular.
So there hasn't been a moment where it's like,
oh, this is where now, I would say in the space of music,
what makes a lot of money?
We're talking about serious money.
It's music and movies, or like shows and so on, and entertainment.
There hasn't been a moment where AI created,
AI was able to create a piece of music,
or a piece of cinema, like Netflix show,
that is, you know, that's sufficiently popular to make a ton of money.
Yeah.
And that moment would be very, very powerful,
because that's like an AI system being used to make a lot of money.
And like direct, of course, AI tools, like even premiere, audio editing,
all the editing, everything I do.
To edit this podcast, there's a lot of AI involved.
I won't, actually, this is a program.
I want to talk to those folks just because I want to nerd out.
It's called Isotope, I don't know if you're familiar with it.
They have a bunch of tools of audio processing,
and they have, I think they're Boston based.
Just, it's so exciting to be, to use it, like on the audio here,
because it's all machine learning.
It's not, because most audio production stuff is like any kind of processing you do,
it's very basic signal processing, and you're tuning knobs and so on.
They have all of that, of course,
but they also have all of this machine learning stuff,
where you actually give it training data,
you select parts of the audio you train on,
you train on it, and it figures stuff out.
It's great.
It's able to detect the ability of it to be able to separate voice and music,
for example, or voice in anything.
It's incredible.
It's clearly exceptionally good at applying these different neural networks models
to separate the different kinds of signals from the audio.
Okay, so that's really exciting.
Photoshop, Adobe, people also use it.
But to generate a piece of music that will sell millions, a piece of art, yeah.
No, I agree.
As I mentioned, I offer my AI class,
and an integral part of this is the project, right?
It's my ultimate favorite part,
because typically we have these project presentations
the last two weeks of the classes right before the Christmas break,
and it adds this cool excitement.
And every time, I'm amazed with some projects that people come up with.
And quite a few of them have some link to arts.
I think last year we had a group who designed an AI producing Hokus, Japanese poems.
Oh, wow.
And some of them, it got trained on the English language.
And some of them, they get to present the top selection.
They were pretty good.
Of course, I'm not as special, but you read them and you see it.
It seems profound.
Yes, it seems reasonable.
So it's kind of cool.
We also had a couple of projects where people tried to teach AI
how to play rock music, classical music, I think, and popular music.
Interestingly enough, classical music was among the most difficult ones.
And of course, if you look at the grand masters of music like Bach,
there is a lot of almost math.
Well, he's very mathematical.
Exactly.
So I would imagine that at least some style of this music could be picked up.
And you have this completely different spectrum of classical composers.
And so it's almost like you don't have to sort of look at the data.
You just listen to it and say, nah, that's not it.
Not yet.
That's how I feel, too.
There's open AI as I think open muse or something like that, the system.
It's cool, but it's not compelling for some reason.
It could be a psychological reason, too.
Maybe we need to have a human being, a tortured soul behind the music.
I don't know.
Yeah, absolutely.
I completely agree.
But whether or not one day we'll have a song written by an AI engine
to be in top charts, musical charts, I wouldn't be surprised.
I wonder if we already have one.
And it just hasn't been announced.
We wouldn't know.
How hard is the multi-protein folding problem?
Is that kind of something you've already mentioned, which is baked into this idea
of greater and greater complexity of proteins, like multi-domain proteins?
Is that basically become multi-protein complexes?
Yes.
Like complexes?
Yes, you got it right.
It has the components of both of protein folding and protein-protein interactions.
Because in order for these domains, many of these proteins, actually,
they never form a stable structure.
One of my favorite proteins, and pretty much everyone who I know,
who works with proteins, they always have their favorite proteins.
So one of my favorite proteins, probably my favorite protein,
the one that I worked when I was a post-doc, is so-called post-synaptic density 95,
PSD95 protein. So it's one of the key actors in the majority of neurological processes
at the molecular level.
And essentially, it's a key player in the post-synaptic density.
So this is the crucial part of the synapse, where a lot of these
chemical processes are happening.
So it has five domains, right?
So five protein domains, pretty large proteins.
I think 600 something, I mean, I said,
but the way it's organized itself, it's flexible, right?
So it acts as a scaffold.
So it is used to bring in other proteins.
So they start acting in the orchestrated manner, right?
And the type of the shape of this protein,
in a way, there are some stable parts of this protein, but there are some flexible.
And this flexibility is built in into the protein
in order to become sort of this multifunctional machine.
So do you think that kind of thing is also learnable through the alpha-fold two kind of approach?
I mean, the time will tell.
Is it another level of complexity?
Is it like how big of a jump in complexity is that whole thing?
To me, it's yet another level of complexity,
because when we talk about protein-protein interactions,
and there is actually a different challenge for this called capri.
And so that is focused specifically on macro-molecular interactions,
protein-protein, DNA, et cetera.
But there are different mechanisms that govern molecular interactions
and that need to be picked up, say, by a machine learning algorithm.
Interestingly enough, we actually participated for a few years in this competition.
We typically don't participate in competitions.
I don't know, don't have enough time, you know, because it's very intensive.
It's a very intensive process.
But we participated back in, you know, about 10 years ago or so.
And the way we entered this competition, so we designed a scoring function, right?
So the function that evaluates whether or not your protein-protein interaction
is supposed to look like experimentally solved, right?
So the scoring function is a very critical part of the model prediction.
So we designed it to be a machine learning one.
And so it was one of the first machine learning-based scoring functions used in capri.
And, you know, we essentially, you know, learned what should contribute,
what are the critical components contributing into the protein-protein interaction.
So this could be converted into a learning problem and thereby it could be learned.
I believe so, yes.
Do you think AlphaFold 2 or something similar to it from DeepMind or somebody else
will result in a Nobel Prize or multiple Nobel Prizes?
So like, you know, obviously, maybe not so obviously,
you can't give a Nobel Prize to a computer program.
You, at least for now, give it to the designers of that program.
But do you see one or multiple Nobel Prizes where AlphaFold 2 is like a large percentage
of what that prize is given for?
Would it lead to discoveries at the level of Nobel Prizes?
I mean, I think we are definitely destined to see the Nobel Prize
becoming sort of to be evolving with the evolution of science.
And the evolution of science is such that it now becomes like really multifaceted, right?
You don't really have like a unique discipline.
You have sort of the a lot of cross disciplinary talks in order to achieve
sort of, you know, really big advancements, you know.
So I think, you know, the computational methods will be acknowledged in one way or another.
And as a matter of fact, you know, they were first acknowledged back in 2013, right?
Where, you know, the first three people were, you know, awarded the Nobel Prize
for studying the protein folding, right, the principle.
And, you know, I think all three of them are computational biophysicists, right?
So, you know, that, I think, is unavoidable, you know.
It will come with a time.
The fact that, you know, alpha fold and, you know, similar approaches,
because again, it's a matter of time that people will embrace this, you know, principle
and we'll see more and more such, you know, such tools coming into play.
But, you know, these methods will be critical in a scientific discovery.
No doubts about it.
On the engineering side, maybe a dark question, but do you think it's possible
to use these machine learning methods to start to engineer proteins?
And the next question is something quite a few biologists are against,
some are for, for study purposes, is to engineer viruses.
Do you think machine learning, like, something like alpha fold could be used to engineer viruses?
So, to answer the first question, you know, it has been, you know,
a part of the research in the protein science, the protein design is, you know,
is a very prominent areas of research.
Of course, you know, one of the pioneers is David Baker and Rosetta algorithm
that, you know, essentially was doing the, the, the nova design
and was used to design new proteins, you know.
And design of proteins means design of functions.
So, like, when you design a protein, you can control, I mean, the whole point of a protein,
with a protein structure comes a function, like, it's doing something.
Correct.
So, you can design different things.
So, you can, yeah, so you can, well, you can look at the proteins from the functional perspective.
You can also look at the proteins from the structural perspective, right?
So, the structural building blocks.
So, if you want to have a building block of a certain shape, you can try to achieve it.
Yes.
By, you know, introducing a new protein sequence and predicting, you know, how it will fold.
So, so with that, I mean, it's, it's a natural, one of the, you know, natural applications of these algorithms.
Now, talking about engineering a virus.
With machine learning.
With machine learning, right?
So, well, you know, so luckily for us, I mean, we don't have that much data, right?
We actually, right now, one of the projects that we are carrying on in the lab is we're trying to develop a machine learning algorithm that determines the, whether or not the current strain is pathogenic.
The current strain of the coronavirus.
Of the virus.
I mean, so, so there are applications to coronaviruses because we have strains of SARS-CoV-2, also SARS-CoV, MERS, that are pathogenic, but we also have strains of other coronaviruses that are, you know, not pathogenic.
I mean, the common cold viruses and, you know, and some other ones, right?
So, so.
Pathogenic meaning spreading.
Oh, pathogenic means actually inflicting damage.
Correct.
There are also some, you know, seasonal versus pandemic strains of influenza, right?
And to determining the, what are the molecular determinant, right?
So, that are built in into the protein sequence, into the gene sequence, right?
So, and whether or not the machine learning can determine those, those components, right?
Oh, interesting.
So, like using machine learning to, that's really interesting to, to, to given, the input is like what the entire, the protein sequence, and then determine if this thing is going to be able to do damage to, to a biological system.
Yeah.
So, so I mean.
It's a good machine learning.
You're saying we don't have enough data for that?
We, I mean, for, for this specific one, we do.
We might actually, you know, have to back up on this because we're still in the process.
There was one work that appeared in bio archive by Eugene Kunin, who is one of these, you know, pioneers in, in, in evolutionary genomics.
And they tried to look at this, but, you know, the methods were sort of standard, you know, supervised learning methods.
And now the question is, you know, can you, you know, advance it further by, by using, you know, not so standard methods?
You know, so there's obviously a lot of hope in, in transfer learning where you can actually try to transfer the information that the machine learning learns about the proper protein sequences, right?
And, you know, so, so there is some promise in going this direction.
But if we have this, it would be extremely useful because then we could essentially forecast the potential mutations that would make a current strain more or less pathogenic.
Anticipate, anticipate them from a vaccine development for treatment, anti any viral drug development.
That would be a very crucial task.
But you could also use that system to then say, how would we potentially modify this virus to make it more pathogenic?
This, that's true.
That's true.
I mean, you know, the, again, the hope is, well, several things, right?
So one is that, you know, it's even if you design a, you know, a sequence, right?
So to carry out the actual experimental biology to ensure that all the components working, you know, is, is a completely different method.
Difficult process.
Yes.
Then the, you know, we've seen in the past, there could be some regulation of the moment the scientific community recognizes that it's now becoming no longer a sort of a fun puzzle to, you know, for machine learning.
Could be a well.
Yes, so then there might be some regulation. So I think back in what 2015, there was, you know, there was an issue on regulating the research on influenza strains, right?
There were several groups, you know, use sort of the mutation analysis to determine whether or not this strain will jump from one species to another.
And I think there was like a half a year moratorium on, on, on the research on, on the paper published until, you know, scientists, you know, analyzed it and decided that it's actually safe.
I forgot what that's called something a function, test a function.
Gain a function.
Gain a function. Yeah.
And gain a function, loss of function. That's right. Sorry.
It's, it's like, let's watch this thing mutate for a while to see like, to see what kind of things we can observe.
I guess I'm not so much worried about that kind of research that there's a lot of regulation.
And if it's done very well and with with competence and seriously, I am more worried about kind of this, you know, the underlying aspect of this question is more like 50 years from now.
Speaking to the Drake equation, one of the parameters in the Drake equation is how long civilizations last.
And that's, that seems to be the most important value actually for calculating if there's other alien intelligence civilizations out there.
That's where there's most variability.
Assuming like if life, if that percentage that life can emerge is like not zero, like if we're a super unique,
then it's the how long we last is basically the most important thing.
So from, from a selfish perspective, but also from a Drake equation perspective, I'm worried about the civilization lasting.
And you kind of think about all the ways in which machine learning can be used to design greater weapons of destruction.
Right. And I mean, one way to ask that if you look sort of 50 years from now, 100 years from now, would you be more worried about natural pandemics or engineered pandemics?
Like who's who's the better designer of viruses, nature or humans if we look down the line?
I think in my view, I would still be worried about the natural pandemics simply because I mean the capacity of the nature producing this.
It does pretty good job, right?
Yes.
And the motivation for using virus engineering viruses for as a weapon is a weird one because maybe you can correct me on this,
but it seems very difficult to target a virus, right?
The whole point of a weapon, the way a rocket works.
If it's starting point, you have an endpoint and you're trying to hit a target to hit a target with a virus is very difficult.
It's basically just right.
It's the target would be the human species.
Oh man.
Yeah.
I have a hope in us.
I'm forever optimistic that we will not, there's no, there's insufficient evil in the world to do to lead that to that kind of destruction.
Well, you know, I also hope that, I mean, that's what we see.
I mean, with the way we are getting connected, the world is getting connected.
I think it helps for the world to become more transparent.
Yeah.
So, so the information spread is, you know, I think it's one of the key things for the, for the society to become more balanced.
Yeah.
One way or another.
This is something that people disagree with me on, but I do think that the kind of secrecy the governments have.
So you're kind of speaking more to the other aspects like research community being more open, companies are being more open.
Government is still like, we're talking about like military secrets.
Yeah.
I think, I think military secrets of the kind that could destroy the world will become also a thing of the 20th century.
It'll become more and more open.
Yeah.
I think nations will lose power in the 21st century, like lose sufficient power to our secrecy.
Transparency is more beneficial than secrecy.
But of course, it's not obvious.
Let's hope so.
Let's hope so that, that, you know, the, the, the, the governments will become more transparent.
What, so we last talked, I think in March or April, what have you learned?
How has your philosophical, psychological, biological worldview changed since then?
Or you've been studying it nonstop from a computational biology perspective.
How is your understanding and thoughts about this virus changed over those months from the beginning to today?
One thing that I was really amazed at how efficient the scientific community was.
I mean, and, you know, even just judging on, on this very narrow domain of, you know, protein structure, understanding the structural characterization of this virus from the components point of view of, you know, whole virus point of view.
You know, if you look at, at SARS, right, the, the, something that happened, you know, less than 20, but, you know, close enough 20 years ago.
And you see what, you know, when it happened, you know, what was sort of the response to by the scientific community, you see that the, the structure characterizations did occur.
But it took several years.
Now, the things that took several years, it's a matter of months.
Right.
So, so we, we see that, you know, the, the, the research pop up.
We are at the unprecedented level in terms of the sequencing.
Right.
Never before we had a single virus sequence so many times.
You know, so which allows us to actually to trace very precisely the sort of the evolutionary nature of this virus, what happens.
And it's not just the, you know, this virus independently of everything is, you know, it's the, you know, the, the sequence of this virus linked anchor to the specific geographic place to specific people because,
you know, the, the, the, our genotype influences also, you know, the, the evolution of this, you know, it's, it's always a host pathogen co evolution that, that, you know, occurs.
It'd be cool if we also had a lot more data about sort of the spread of this virus, not maybe, well, it'd be nice if we had it for like contact tracing purposes for this virus, but it'd be also nice if we had it for the study for future virus.
To be able to respond and so on.
Well, but it's already nice that we have geographical data and the basic data from individual humans.
Yeah.
Exactly.
No, I think contact tracing is, is, is obviously a key component in understanding the spread of this virus.
We, there is also, there is a number of challenges, right?
So X price is one of them we, we, you know, just recently to, you know, took a part of this competition.
It's the prediction of the, of the number of infections in different regions.
So, and, you know, obviously the, the AI is the main topic in those predictions.
Yeah, but it's still the data, I mean, that's, that's a competition, but the, the data is weak on the training.
Like it's, it's great.
It's much more than probably before, but like it would be nice if it was like really rich.
I talked to Michael Mina from, from Harvard.
I mean, he dreams that the community comes together with like a weather map to wear of viruses, right?
Like really high resolution sensors on like how from person to person, the viruses that travel, all the different kinds of viruses, right?
Because there's, there's, there's a ton of them.
And then you'll be able to tell the story that you've spoken about of the evolution of these viruses, like day to day mutations that are occurring.
I mean, that would be fascinating just from a perspective of study and from the perspective of being able to respond to future pandemics.
That's ultimately what I'm worried about.
People love books.
Is there, is there some three or whatever number of books, technical fiction, philosophical that, that brought you joy in life, had an impact on your life, and maybe some that you would recommend others.
So I'll give you three very different books.
And I also have a special runner up and honorable matching.
Yeah, it's, yeah, I wouldn't, I mean, it's, it's an audio book.
And that's, there's some specific reason behind it.
So, you know, so the first book is, you know, something that sort of impacted my earliest stage of life.
And I probably not going to be very original here.
It's Bulgakov's master and Margarita.
So that's probably, you know,
Well, not for a Russian, maybe it's not super original, but it's, you know, it's a really powerful book for even in English.
So it is incredibly powerful.
And I mean, it's the way it ends, right?
So it's, it's, I still have goosebumps when I read the very last sort of, it's called prologue, where it's just so powerful.
What impact did you have on your, what ideas, what insights did you get from it?
I was just taken by, you know, by the, the fact that you have those parallel lives apart from many centuries, right?
And somehow they, they got sort of intertwined into one story.
And, and that's to me was fascinating. And, you know, of course, the, you know, the romantic part of this book is like, it's not just, you know, romance.
It's like the romance impart by sort of magic, right?
And that, and, and, and, and maybe on top of that, you have some irony, which unavoidable, right?
Because it was that, you know, the Soviet time.
But it's very, it's very, it's deeply Russian. So that's the, the wit, the humor, the pain, the love, all of that is one of the books that kind of captures something about Russian culture that people outside of Russia should probably read.
What's the, what's the second one?
So, so the second one is again, another one that it happened. I read it later in my life. I think I read it first time when I was a graduate student.
And that's the Solzhenitsyn's cancer ward. That is amazingly powerful book.
What is it about?
It's about, I mean, essentially based on, on, you know, Solzhenitsyn was diagnosed with cancer when he was reasonably young and he, he made a full recovery.
But, you know, so, so this is about a person who was sentenced for life in one of these, you know, camps.
And he had some cancer. So he was, you know, transported back to one of these Soviet republics, I think, you know, South Asian republics.
And the book is about, you know, his experience being a prisoner, being a, you know, a patient in the cancer clinic in a cancer ward surrounded by people, many of which die, right?
But in a way, you know, the way, you know, it reads, I mean, first of all, later on, I read the accounts of the, of the doctors who describe these, you know, the experiences, you know, in the book by the patient as, as incredibly accurate.
Right. So, so, you know, I read that there was, you know, some doctors saying that, you know, every single doctor should read this book to understand what the patient feels.
But, you know, again, as many of the Solzhenitsyn, Solzhenitsyn's books, it has multiple levels of complexity.
And obviously, the, you know, if you look above the cancer and the patient, I mean, the tumor that was growing and then disappeared in his, you know, in his body with some consequences.
I mean, this is, you know, allegorically, the Soviet and, you know, and he actually, he, you know, when he was asked, he said that this is what made him think about this, you know, how to combine these experiences.
Him being a part of the, you know, of the Soviet regime, also being a part of the, of the, you know, of someone sent to the, to Gulag camp, right?
And also someone who experienced cancer in his life, you know, the Gulag archipelago and this book, these are the works that actually made him, you know, receive a Nobel Prize.
But, you know, to me, I, I've, you know, I've read different other, you know, books by Solzhenitsyn.
This one is, to me, is the most powerful one.
And by the way, both this one and the previous one you write in Russian?
Yes. Yes. So now there is the third book is, is an English book. And it's completely different.
So, so, you know, we're switching the gears completely. So this is the book, which it's not even a book.
It's a, it's an essay by Jonathan Neumann called The Computer and the Brain.
And that was the book he was writing, knowing that he, he was dying of cancer.
So, so the book was released back. It's a very thin book, right? But the, the power, the intellectual power in, in this book, in this essay is incredible.
I mean, you probably know that for Neumann is considered to be one of these biggest thinkers, right?
So the, his intellectual power was incredible, right? And you can actually feel this power in this book where, you know, the person is writing knowing that he will be, you know, he will die.
The book actually got published only after his death back in 1958. He died in 1957.
And, but so, so he tried to put as many ideas that, you know, he still, you know, hadn't realized.
And, you know, so, so this book is very difficult to read because, you know, every single paragraph is just compact, you know, is, is filled with these ideas and, you know, the ideas are incredible.
You know, nowadays, you know, so, so he tried to put the parallels between the brain computing power, the neural system and the computers, you know, as they were.
Do you remember what year he was working on? It's like, 57.
57.
So, so that was right during his, you know, when he was diagnosed with cancer and he was essentially.
Yeah, he's one of those. There's a few folks people mentioned. I think Ed Whitton is another that like every, but everyone that meets them, they say he's just an intellectual powerhouse.
Yes.
Okay, so who's the honorable mention?
So, so, so, and this is, I mean, the reason I put it sort of in a separate section because this is a book that I reasonably listened, recently listened to.
So, so it's an audio book. And this is a book called Lab Girl by Hope Jarren.
So Hope Jarren, she is a scientist. She's a geochemist that essentially studies the, the fossil plants.
And so she uses the fossil, the chemical analysis to understand what was the climate back in, you know, in 1000 years, hundreds of 1000 years ago.
And so something that incredibly touched me by this book, it was narrated by the author.
Nice.
And it's an incredibly personal story, incredibly.
So certain parts of the book, you could actually hear the author crying.
And that to me, I mean, I never experienced anything like this, you know, reading the book, but it was like, you know, the, the connection between you and the author.
And I think this is, you know, this is really a must read, but even better, a must listen to audio book for anyone who wants to learn about sort of, you know, academia, science research in general,
because it's a very personal account about her becoming a scientist.
So we're just before New Year's, you know, we talked a lot about some difficult topics of viruses and so on.
Do you have some exciting things you're looking forward to in 2021, some New Year's resolutions, maybe silly or fun, or something very important and fundamental to the world of science or something completely unimportant.
Well, well, I'm definitely looking forward to towards, you know, things becoming normal.
Right.
So, yes, so I really miss traveling every summer.
I go to a international summer school is called the School for Molecular and Theoretical Biology.
It's held in Europe.
It's organized by very good friends of mine.
And this is the school for gifted kids from all over the world.
And they're incredibly bright.
It's like every time I go there, it's like, you know, it's a highlight of the year.
And we couldn't make it this August.
So we did this school remotely, but it's different.
So I am definitely looking forward to next August coming there.
I also mean, you know, one of the one of my, you know, personal resolutions, I realized that, you know, being in, you know, in-house and working from home, you know, I realized that actually I apparently missed a lot, you know, spending time with my family, believe it or not.
So you typically, you know, with all the research and, you know, and teaching and everything related to the academic life, I mean, you get distracted.
And so, so, you know, you don't feel that, you know, the fact that you are away from your family doesn't affect you because you are, you know, naturally distracted by other things.
And, you know, this time I realized that, you know, that that's so important, right?
Spending your time with the family, with your kids.
And so that would be my new year resolution in actually trying to spend as much time as possible.
Even when the world opens up, yeah.
That's a beautiful message.
That's a beautiful reminder.
I asked you if there's a Russian poem you could read that I could force you to read and you said, okay, fine, sure.
Do you mind, do you mind reading?
And you're like, you said that no paper needed.
Nope.
So yeah, so this poem was written by my namesake, another Dmitry, Dmitry Kemerfeldt.
And is a, you know, it's a recent poem and it's, it's called Sorceress, Viedma, in Russian, or actually Kaldunia.
So that's sort of another sort of connotation of Sorceress or witch.
And I really like it.
And it's one of just a handful poems I actually can recall by heart.
I also have a very strong association when I read this poem with a master Margarita, the main female character Margarita.
And also it's, you know, it's about, you know, it's happening about the same time we're talking now.
So around New Year, around Christmas.
Do you mind reading it in Russian?
I'll give it a try.
So you took your eyes off your chest, that anyone who got down to grace was ready to give this witchish connection without looking at the devil's soul.
There was a thief hanging around in the bushes.
But I, without any prejudices, ran away to feel your crazy breath on my lips.
So that your skin, with your tongue, with your ribs, on someone else's, on a ghostly land,
can remember whether you were on the ground or on the ground, in the white in the south, in the white in the blue, in the white in the blue.
That's beautiful.
I love how it captures a moment of longing and maybe love even.
To me, it has a lot of meaning about, you know, this something that is happening, something that is far away, but still very close to you.
And yes, it's the winter.
There's something magical about winter, isn't it?
What is the, well, I don't know.
I don't know how to translate it, but a kiss in winter is interesting.
Lips in winter and all that kind of stuff.
It's beautiful.
I mean, Russian as a way.
As a reason, Russian poetry is just, I'm a fan of poetry in both languages, but English doesn't capture some of the magic that Russian seems to.
So thank you for doing that.
That was awesome.
Dmitry, it's great to talk to you again.
It's contagious how much you love what you do, how much you love life.
So I really appreciate you taking the time to talk today.
And thank you for having me.
Thanks for listening to this conversation with Dmitry Korkin.
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