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So how are we going to beat
this novel coronavirus?
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By using our best tools:
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our science and our technology.
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In my lab, we're using
the tools of artificial intelligence
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and synthetic biology
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to speed up the fight
against this pandemic.
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Our work was originally designed
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to tackle the antibiotic
resistance crisis.
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Our project seeks to harness
the power of machine learning
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to replenish our antibiotic arsenal
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and avoid a globally devastating
postantibiotic era.
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Importantly, the same
technology can be used
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to search for antiviral compounds
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that could help us fight
the current pandemic.
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Machine learning is turning
the traditional model of drug discovery
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on its head.
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With this approach,
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instead of painstakingly testing
thousands of existing molecules
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one by one in a lab
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for their effectiveness,
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we can train a computer
to explore the exponentially larger space
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of essentially all possible molecules
that could be synthesized,
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and thus, instead of looking
for a needle in a haystack,
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we can use the giant magnet
of computing power
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to find many needles
in multiple haystacks simultaneously.
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We've already had some early success.
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Recently, we used machine learning
to discover new antibiotics
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that can help us fight off
the bacterial infections
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that can occur alongside
SARS-CoV-2 infections.
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Two months ago, TED's Audacious Project
approved funding for us
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to massively scale up our work
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with the goal of discovering
seven new classes of antibiotics
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against seven of the world's
deadly bacterial pathogens
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over the next seven years.
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For context:
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the number of new class of antibiotics
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that have been discovered
over the last three decades is zero.
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While the quest for new antibiotics
is for our medium-term future,
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the novel coronavirus poses
an immediate deadly threat,
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and I'm excited to share that we think
we can use the same technology
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to search for therapeutics
to fight this virus.
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So how are we going to do it?
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Well, we're creating
a compound training library
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and with collaborators applying these
molecules to SARS-CoV-2-infected cells
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to see which of them exhibit
effective activity.
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These data will be use to train
a machine learning model
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that will be applied to an in silico
library of over a billion molecules
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to search for potential
novel antiviral compounds.
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We will synthesize and test
the top predictions
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and advance the most promising
candidates into the clinic.
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Sound too good to be true?
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Well, it shouldn't.
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The Antibiotics AI Project is founded
on our proof of concept research
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that led to the discovery
of a novel broad-spectrum antibiotic
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called Halocin.
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Halocin has potent antibacterial activity
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against almost all antibiotic-resistant
bacterial pathogens,
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including untreatable
panresistant infections.
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Importantly, in contrast
to current antibiotics,
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the frequency at which bacteria
develop resistance against Halocin
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is remarkably low.
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We tested the ability of bacteria
to evolve resistance against Halocin
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as well as Cipro in the lab.
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In the case of Cipro,
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after just one day, we saw resistance.
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In the case of Halocin,
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after one day,
we didn't see any resistance.
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Amazingly, after even 30 days,
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we didn't see any resistance
against Halocin.
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In this pilot project, we first tested
roughly 2,500 compounds against E. coli.
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This training set included
known antibiotics,
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such as Cipro and penicillin,
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as well as many drugs
that are not antibiotics.
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These data we used to train a model
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to learn molecular features
associated with antibacterial activity.
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We then applied this model
to a drug-repurposing library
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consisting of several thousand molecules
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and asked the model to identify molecules
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that are predicted
to have antibacterial properties
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but don't look like existing antibiotics.
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Interestingly, only one molecule
in that library fit these criteria,
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and that molecule
turned out to be Halocin.
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Given that Halocin does not look
like any existing antibiotic,
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it would have been impossible for a human,
including an antibiotic expert,
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to identify Halocin in this manner.
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Imagine now what we could do
with this technology
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against SARS-CoV-2.
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And that's not all.
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We're also using the tools
of synthetic biology,
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tinkering with DNA
and other cellular machinery,
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to serve human purposes
like combating COVID-19,
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and of note, we are working
to develop a protective mask
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that can also serve
as a rapid diagnostic test.
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So how does that work?
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Well, we recently showed
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that you can take the cellular
machinery out of a living cell
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and freeze-dry it along with
RNA sensors onto paper
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in order to create low-cost
diagnostics for Ebola and Zika.
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The sensors are activated when
they're rehydrated by a patient sample
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that could consist of blood
or saliva, for example.
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It turns out, this technology
is not limited to paper
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and can be applied
to other materials, including cloth.
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For the COVID-19 pandemic,
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we're designing RNA sensors
to detect the virus
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and freeze-drying these
along with the needed cellular machinery
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into the fabric of a face mask,
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where the simple act of breathing,
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along with the water vapor
that comes with it,
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can activate the test.
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Thus, if a patient is infected
with SARS-CoV-2,
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the mask will produce
a fluorescent signal
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that could be detected by a simple,
inexpensive handheld device.
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In one or two hours, a patient
could thus be diagnosed
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safely, remotely and accurately.
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We're also using synthetic biology
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to design a candidate
vaccine for COVID-19.
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We are repurposing the BCG vaccine,
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which had been used against TB
for almost a century.
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It's a live attenuated vaccine,
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and we're engineering it
to express SARS-CoV-2 antigens,
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which should trigger the production
of protective antibodies
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by the immune system.
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Importantly, BCG
is massively scalable
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and has a safety profile that's among
the best of any reported vaccine.
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With the tools of synthetic biology
and artificial intelligence,
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we can win the fight
against this novel coronavirus.
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This work is in its very early stages,
but the promise is real.
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Science and technology
can give us an important advantage
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in the battle of human wits
versus the genes of superbugs,
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a battle we can win.
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Thank you.
Erin Gregory
English transcript correction:
Halocin --> halicin