A new type of medicine, custom-made with tiny proteins | Christopher Bahl

80,787 views ・ 2020-02-19

TED


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譯者: Lilian Chiu 審譯者: 易帆 余
00:13
I'm a protein designer.
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我是蛋白質設計師。
00:16
And I'd like to discuss a new type of medicine.
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我想要談的是一種新的藥物。
00:19
It's made from a molecule called a constrained peptide.
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它是由一種分子製造, 叫做拘束胜肽。
00:24
There are only a few constrained peptide drugs available today,
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現今只有少數幾種拘束胜肽藥物,
但在接下來十年會有 更多出現在市場上。
00:27
but there are a lot that will hit the market in the coming decade.
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咱們來探討這些新藥品 怎麼製成、有何不同,
00:30
Let's explore what these new medicines are made of,
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00:32
how they're different and what's causing this incoming tidal wave
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以及是什麼原因造成 這波另人興奮的新藥浪潮。
00:35
of new and exciting medicines.
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00:38
Constrained peptides are very small proteins.
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拘束胜肽是非常小的蛋白質。
00:42
They've got extra chemical bonds that constrain the shape of the molecule,
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它們有額外的化學鍵 可以拘束分子的形狀,
00:45
and this makes them incredibly stable
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因此它們非常穩定,
00:47
as well as highly potent.
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同時效力也非常強。
00:50
They're naturally occurring, our bodies actually produce a few of these
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它們是天然的,人體就會產生幾種,
能協助我們對抗細菌性、 霉菌性,和病毒性感染。
00:53
that help us to combat bacterial, fungal and viral infections.
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00:56
And animals like snakes and scorpions
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蛇和蝎子這些動物
00:58
use constrained peptides in their venom.
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在毒液中就有拘束胜肽。
01:00
Drugs that are made of protein are called biologic drugs.
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用蛋白質做成的藥物稱為生物藥。
01:03
So this includes constrained peptides,
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生物藥包括拘束胜肽,
01:05
as well as medicines like insulin
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以及胰島素這類藥物,
01:08
or antibody drugs like Humira or Enbrel.
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或是阿達木單抗、 依那西普等抗體藥物。
01:11
And in general, biologics are great,
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一般來說,生物藥很好,
01:14
because they avoid several ways that drugs can cause side effects.
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因為它們有好幾種機制 可以避免掉藥物造成的副作用。
01:19
First, protein.
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首先,蛋白質。
01:20
It's a totally natural, nontoxic material in our bodies.
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它是我們體內完全天然、 無毒性的材料。
01:23
Our cells produce tens of thousands of different proteins,
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我們的細胞會產生 數萬種不同的蛋白質,
01:26
and basically, all of our food has protein in it.
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我們所有的食物 基本上都含有蛋白質。
01:29
And second, sometimes drugs interact with molecules in your body
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第二,有時,
一般藥物在體內會和分子 發生你不想要的作用。
01:33
that you don't want them to.
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01:34
Compared to small molecule drugs,
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相較於小分子藥物,
01:36
and by this I mean regular drugs, like aspirin,
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我指的是一般藥物,如阿斯匹靈,
01:39
biologics are quite large.
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生物藥算是相當大的。
01:41
Molecules interact when they adopt shapes that fit together perfectly.
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分子的形狀能完美符合時 就會發生交互作用。
01:45
Much like a lock and key.
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很像鎖和鑰匙。
01:46
Well, a larger key has more grooves,
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比較大的鑰匙有比較多溝槽,
01:48
so it's more likely to fit into a single lock.
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所以比較有可能符合一個鎖。
01:52
But most biologics also have a flaw.
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但,大部分的生物藥都有個瑕疵。
01:54
They're fragile.
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它們很脆弱。
01:56
So they're usually administered by injection,
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所以通常會用注射的,
01:58
because our stomach acid would destroy the medicine
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因為如果用吃的, 胃酸會破壞這種藥。
02:00
if we tried to swallow it.
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拘束胜肽則相反。
02:02
Constrained peptides are the opposite.
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02:04
They're really durable, like regular drugs.
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它們的耐受度跟一般藥物一樣強。
02:06
So it's possible to administer them using pills, inhalers, ointments.
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所以是有可能用藥丸、吸入器、 軟膏的方式來服用塗抹這類藥物。
02:11
This is what makes constrained peptides so desirable for drug development.
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這就是為什麼在藥物發展上 拘束胜肽十分讓人滿意。
02:16
They combine some of the best features
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它們把小分子和生物藥的優點
02:17
of small-molecule and biologic drugs into one.
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都結合在一起了。
02:21
But unfortunately, it's incredibly difficult
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但,不幸的是,我們非常難將
02:24
to reengineer the constrained peptides that we find in nature
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大自然中找到的拘束胜肽
重新再造為新藥物。
02:27
to become new drugs.
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02:28
So this is where I come in.
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於是該我登場了。
02:30
Creating a new drug is a lot like crafting a key
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創造新藥物很像是針對某個鎖
02:33
to fit a particular lock.
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刻出符合的鑰匙。
02:36
We need to get the shape just right.
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我們必須要把形狀做對。
02:37
But if we change the shape of a constrained peptide by too much,
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但,若把拘束胜肽的 形狀改變太多,
02:40
those extra chemical bonds are unable to form
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那些額外的化學鍵就無法形成,
02:43
and the whole molecule falls apart.
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整個分子就會崩壞。
02:45
So we needed to figure out how to gain control over their shape.
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所以我們必須要想辦法 控制它們的形狀。
02:48
I was part of a collaborative scientific effort
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我參與了一項科學合作計畫,
02:50
that spanned a dozen institutions across three continents
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橫跨三個國家十多個機構,
02:54
that came together and solved this problem.
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大家集結起來要解決這個問題。
02:57
We took a radically different approach from previous efforts.
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我們根據先前經驗採用了 一個非常不同的方式。
03:00
Instead of making changes to the constrained peptides
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我們不是去改變 在大自然中找到的拘束胜,
03:03
that we find in nature,
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我們是想辦法從無到有 打造出新的拘束胜肽。
03:04
we figured out how to build new ones totally from scratch.
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03:07
To help us do this,
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為此,我們開發了 開放程式碼的胜肽設計軟體,
03:08
we developed freely available open-source peptide-design software
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讓任何人都可以自由取用來做設計。
03:12
that anyone can use to do this, too.
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03:13
To test our method out,
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為了測試我們的方法, 我們先生成一系列的拘束胜肽,
03:15
we generated a series of constrained peptides
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03:18
that have a wide variety of different shapes.
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有各式各樣的形狀。
03:20
Many of these had never been seen in nature before.
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當中有許多是 大自然中前所未見的。
03:22
Then we went into the laboratory and produced these peptides.
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接著,我們進入實驗室, 製造出這些肽。
03:25
Next, we determined their molecular structures,
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然後,我們用實驗 來決定它們的分子結構,
03:28
using experiments.
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03:29
When we compared our designed models
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把我們設計的模型 和真實的分子結構做比較後,
03:31
with the real molecular structures,
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03:33
we found that our software can position individual atoms
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我們發現,我們的軟體 可以定位個別原子,
03:36
with an accuracy that's at the limit of what's possible to measure.
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且精準到超過能測量的極限。
03:39
Three years ago, this couldn't be done.
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三年前,這還是不可能的。
03:42
But today, we have the ability to create designer peptides
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但,現今,我們有能力 可以創造出客製化的胜肽,
03:45
with shapes that are custom-tailored for drug development.
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可以客製化它們的形狀做藥物開發。
03:48
So where is this technology taking us?
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這項技術會引領我們到哪裡?
03:51
Well, recently,
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最近,我和同事設計出的拘束胜肽
03:52
my colleagues and I designed constrained peptides
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03:54
that neutralize influenza virus,
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能夠殺死流感病毒、
03:58
protect against botulism poisoning
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避免肉毒中毒,
04:01
and block cancer cells from growing.
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及阻擋癌症細胞生長。
04:03
Some of these new drugs
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其中一些新藥物已經 用實驗室動物做過臨床前試驗,
04:04
have been tested in preclinical trials with laboratory animals.
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04:07
And so far, they're all safe and highly effective.
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目前,它們都很安全且非常有效。
04:12
Constrained peptide design is a cutting-edge technology,
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拘束胜肽設計是一項先進技術,
04:15
and the drug development pipeline is slow and cautious.
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而藥物開發的過程既緩慢又謹慎。
04:17
So we're still three to five years out from human trials.
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所以還要三到五年才能做人體試驗。
04:20
But during that time,
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但,在那期間,
04:21
more constrained peptide drugs
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會有更多拘束胜肽藥物 進入藥物開發過程。
04:23
are going to be entering the drug development pipeline.
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04:25
And ultimately, I believe that designed peptide drugs
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最終,我相信客製化的拘束胜肽藥物
04:30
are going to enable us all to break free
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將讓我們有能力擺脫疾病的拘束。
04:32
from the constraints of our diseases.
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04:34
Thank you.
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謝謝。
04:35
(Applause)
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(掌聲)
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