Can Genetic Engineering Help Us In the Fight Against COVID19

ninth grade i was invited to this

biology conference at my school and i

was really excited about attending it

because i got to skip

all my classes and they gave us free

pizza for lunch heck yeah

now in one of the presentations about

the study of diseases one student from

the audience asked

why do scientists try to cure rare

diseases more than common diseases

and to that the lecturer said well i

guess i don’t really know

the thing about common diseases is that

there are so many

factors that influence the final result

some can include genetics

diet or maybe something no one knows

about

yet and i emphasize yet because that’s

what science is about right guys

it’s about discovering and testing and

innovating and now

especially during the age of technology

the 21st century

the power of science has been more

important than ever

there is a deathly pandemic of sars kobe

2 that has taken over our lives

and has made life a lot more boring than

it usually is

but what if i told you that your life

will be able to get back to the normal

amount of boring it was

and if your life wasn’t that boring

during your pandemic that’s up to you

but how well a vaccine is coming but

also a new technology that will be able

to detect coping 19

faster and cheaper the super cool thing

is that this technology that i want to

talk to you guys about today

is already being retailed across the

nation

but let’s backtrack and let me introduce

you to how it all started

with the discovery of crispr now many of

you might have heard the name

crisper before what is it not a new lace

chip flavor

although it definitely should be crisper

is short for clustered regularly

interspaced short palindromic repeats

quite a mouthful i know but that’s what

i’m here for so let’s break it down

according to quantum magazine the

discovery of christopher started in 1987

when a few scientists from osaka

university in japan found something

peculiar

they looked at a specific gene a single

unit of heredity something we get from

both our mom

and our dad and this specific gene the

iaf gene was from the gut of an e coli

microbe

microbe being tiny living things that

are everywhere

and yes everywhere under your bed in

your mouth

i think you just followed one so when

the scientists sequence the dna

the genetic material that makes us who

we are and its surroundings

they expect it to find proteins

molecules that sped up chemical

reactions functioning like a light

switch

on the legs on transcription or copying

of our body’s genetic material into a

piece of rna

a squiggly line also made out of genetic

material that primarily helps make

proteins occurs

but when that light is off this process

stops

however what the scientists found was

that near the ef can make five

identical segments of dna unique spacers

which are 32

random dna base blocks so imagine 32

random lego blocks piling up on each

other

and a bunch of jeans which they dubbed

cash genes

now if anyone likes hamburgers i know i

do

i think i may have an easier way of

explaining this concept

imagine a sandwich filled with five

patties which are your short palindromic

repeats

and palindromic is like the word race

car race car is publishing forwards and

backwards just like the dna based blocks

separated with different types of cheese

which is your inter-space

part of crisper and let’s hope the

cheese doesn’t melt

moldy and on the top let’s say there’s

about four-ish olives and the more

all the more olives the better yeah yeah

popular opinion

so after a few years many more

scientists found the same type of

genetic sandwiches like the ones in e

coli

so after a bunch of testing and

hypothesizing

the function of crispr was discovered

okay so the 100 question is what does

crispr do

what scientists found according to the

nature journal 33 years ago

was a defense mechanism by microbes that

would capture small pieces

of dna from invading viruses store that

in those

interspace repeats and if they ever saw

that virus again

they’d cut the virus dna apart making

the bacteria

safe however in the lab it’s a little

different because the purpose is to edit

our body’s genome

almost like a cut and paste function but

in real life

according to the national institutes of

health the two main components

include cas9 a dna cutting protein and a

guide rna

together they locate a specific part of

the genome that we’re trying to find

online that specific target dna sequence

and from there

they have a few options they’ve either

cut the nucleotides

the bases of genetic molecules

deactivating the entire gene

block or induced transcription and

transcription once again

is the copying of our body’s genetic

material into

a easier to create proteins molecule

or they can paste or substitute a new

nucleotide which can lead to preventing

diseases according to the cystic

fibrosis foundation

one base block error in the cftr gene

can be

fixed using crispr cas9 genome editing

another disease that will majorly

benefit is sickle cell disease in which

once again

only one base is mutated forming defects

in the way blood cells are formed

all right let’s switch gears and talk

about genetic engineering and the

context of the problems our world is

facing

right now the code 19 pandemic has

impacted the world on a

massive scale and is arguably the most

destructive virus

of this generation the cases and deaths

have reached new highs

most notably the united states with a

recorded carotid virus death number

of around 320 000 people and

cases of about 17.7 million people

and these numbers are from the 20th of

december so they have definitely

increased one major problem countries

face with the growing infection rate is

a lack of contract tracers

and lack of testing however according to

biological procedures online

sherlock and no not sherlock holmes

although he’s pretty cool too but

sherlock a genetic engineering solution

will be able to detect kobit 19

using crispr cast 13. okay let’s recap a

little

we already know that crispr is the short

interspace repeats in a microorganism

and that cas9 a dna cutting protein is

bound to a guide rna to do so

and once again that guide helps us find

the specific target dna sequence that we

are looking for

cast 13 is a cousin of cast 9 that can

be harnessed to actually detect

human disease but probably early rude

cousin because cast man’s getting

all the attention according to the

mcgovern institute a community of mit

scientists

and microbes and bacteria cast 13 is

also bound

to a guide rna to detect viral rna

and once that viral rna is bound cast 13

starts a process called collateral

cleavage which

means it cuts up any rna segment it

detects

well doesn’t that seem unnecessary what

does cutting up

random rna segments do with anything

well surprisingly this is the meat of

sherlock’s capabilities

so how does sherlock work first

researchers take a sample of a patient

who possibly has

a viral infection then they amplify the

levels of rna in that sample and add

reporters which

are sensitive to cast 13. next many

engineered cast 13s are added into the

sample with

a guide rna to detect that viral rna

and once that viral rna is bound cast 13

starts the process of collateral

cleavage once again

means it cuts up anything in its path

including the reporters

well why the reporters the reporters

being cleared is what actually detects

the virus

each reporter has a unique label and

when caster team cleaves it into two

they create a unique signal which can

help detect

whether a person has a virus or not so

imagine a pregnancy test

well what does a pregnancy test even do

according to the national health service

one

early sign of being pregnant is the

body’s production of the hormone hcg

or human chronic gonadotropin in a

woman’s blood and urine

and when their urine comes in contact

with that specially treated strip

the test detects whether or not hcg was

detected

now this process is very similar to what

happens with the cleaved reporters

once the reporters are sliced they enter

a commercial flow detection system

just like the pregnancy test and

when and if the sample is negative for

that virus

the reporters collect at the first

detection line however if it’s positive

they collect at a different detection

line making a diagnosis very easy

to spot just like the darker red and

therapeutic lines on a pregnancy test

detecting covid19 will be significantly

easier and will start a path of

increased recovery

in our pandemic as i said before and as

i’m saying now

science is amazing we started with an

unknown unidentifiable gene and a random

bacterium

and created it into a certified fruit

ninja warrior

but instead of cutting fruit we’re

cutting jeans

discovery is possible innovation is

always occurring and solutions

will always be created okay so let’s

answer that student’s question

why do scientists try to cure rare

diseases more than common diseases

the lecturer should have said well it’s

because our world is filled with

peculiarities that will one day

be able to cure the deathliest diseases

but until then we just gotta wait

so time time is the answer to her

question and that will be the answer for

our pandemic

as well

九年级时,我被邀请

参加我学校的这个生物学会议,我

很高兴能参加,

因为我不得不跳过

所有的课,他们给了我们免费的

比萨作为午餐,哎呀,

现在在

关于疾病研究的演讲之一中

听众中的学生问

为什么科学家们试图治愈罕见

病而不是常见病

,对此讲师说得很好我

想我真的不

知道常见病的事情

是影响最终结果的因素太多了

一些 可以包括遗传

饮食或者可能还没有人知道的东西

,我强调,因为这

就是科学是关于正确的人的,

它是关于发现、测试和

创新的,现在

尤其是在 21 世纪的技术时代

,科学的力量变得更加

重要 比以往任何

时候都发生了一场致命的 sars kobe 2 大流行

,它接管了我们的生活

,让生活比平时更无聊

但是什么 如果我告诉您,您的生活

将能够恢复到正常

的无聊程度,

并且在大流行期间您的生活是否不那么无聊

,这取决于您,

但疫苗的研制情况如何,

以及一项新技术 将能够

更快、更便宜地检测到应对 19 最酷的

是,我

今天想和你们谈谈的这项技术

已经在全国范围内零售,

但让我们回过头来,让我向

你介绍这一切是如何开始

的 现在发现crispr

你们中的许多人可能已经听说过crisper 这个名字

之前它不是一种新的花边

薯片味道

虽然它绝对应该是更脆的,

是聚集的定期

间隔短回文重复的缩写,

我知道,但这就是

我在这里 因此,让我们根据量子杂志对其进行分解

。 christopher 的发现始于 1987 年,

当时日本大阪大学的几位科学家

发现了一些奇特的东西,

他们看着一个特定的 ic 基因 一个单一

的遗传单位 我们从妈妈和爸爸那里得到的东西

,而这个特定的基因

iaf 基因来自大肠杆菌微生物的肠道 微生物

是无处不在的微小生物,是的,无处不在

我想你只是跟着一个,所以

当科学家们对

使我们成为我们自己的遗传物质

及其周围环境进行 dna 测序时,

他们希望它能找到

加速化学

反应的蛋白质分子,就像腿上的电灯

开关一样

,在转录或

复制 我们身体的遗传物质变成了

一段 rna

一条波浪线也是由遗传

物质制成的,主要有助于

产生蛋白质,

但是当光线熄灭时,这个过程就会

停止,

但是科学家们发现

,在 ef 附近可以产生五个

相同的 dna 片段 独特的

垫片是 32 个

随机的 dna 基础块,所以想象一下 32 个

随机的乐高积木堆在一起

,还有一堆他们配音的牛仔裤 现在编辑

现金基因

如果有人喜欢汉堡包我知道我

喜欢

我想我可能有一个更简单的方法来

解释这个概念

想象一个三明治里有五个

馅饼这是你的短回文

重复

和回文就像这个词

赛车赛车正在向前出版 和

向后就像基于 dna 的块

用不同类型的奶酪分开,

这是你

的保鲜盒的空间部分,让我们希望

奶酪不会融化

发霉,在顶部让我们说

大约有四个橄榄,而且

更多 橄榄越多越好 是的 是的

流行的观点

所以几年后,更多的

科学家发现了与

大肠杆菌中的基因三明治相同类型的基因三明治

所以经过一系列测试和

假设

crispr的功能被发现

好的 所以100个问题是什么

科学家们在

33 年前根据《自然》杂志发现,crispr 的作用

是一种微生物防御机制,

可以捕获

来自 invadi 的小块 dna ng 病毒将其存储

在那些

空间重复序列中,如果他们再次看到

该病毒,

他们会将病毒 dna 切割成

安全的细菌,但是在实验室中它有点

不同,因为其目的是编辑

我们身体的基因组,

几乎就像一个切口和 粘贴功能,但

根据美国国立卫生研究院的说法,在现实生活中,

这两个主要成分

包括 cas9 一种 dna 切割蛋白和一种

引导 rna

,它们一起定位

了我们试图在网上找到的基因组的特定部分,

即特定的目标 dna 序列

和 从那里

他们有几个选择,他们要么

切割核苷酸

,基因分子的碱基,

使整个基因块失活,

要么诱导转录,

转录

再次将我们身体的遗传

物质复制成

更容易产生的蛋白质分子,

或者他们可以粘贴 或

根据囊性

纤维化基础的

一个碱基块错误替换一种新的核苷酸可以预防疾病 cftr 基因

可以

使用crispr cas9 基因组编辑修复

另一种主要

受益的疾病是镰状细胞病,其中

再次

只有一个碱基发生突变,形成

血细胞形成方式的缺陷

好吧让我们换个角度

谈谈基因工程和

我们的世界目前面临的问题的背景

19 号代码大流行已经

大规模影响了世界,可以说

是这一代最具破坏性的病毒 病例和死亡人数

已达到新高,

最引人注目的是美国有

记录的颈动脉

大约 320 000 人的病毒死亡人数和

大约 1770 万人的病例

,这些数字是从

12 月 20 日开始的,因此它们肯定

增加了各国面临的感染率不断增长的一个主要问题

是缺乏合同追踪者

和缺乏测试然而 根据

生物程序在线

夏洛克而不是夏洛克福尔摩斯

虽然他也很酷但是

sherlock 基因工程解决方案

将能够

使用crispr cast 13 检测 kobit 19。好吧,让我们回顾一下

我们已经知道,crispr 是

微生物中的短间隔重复序列,

并且 cas9 一种 dna 切割

蛋白与引导 rna 结合 所以

该指南再一次帮助我们

找到我们正在寻找的特定目标 dna 序列

cast 13 是 cast 9 的表亲,

可以用来实际检测

人类疾病,但可能是早期粗鲁的

表亲,因为 cast man 得到了

所有的关注

麦戈文研究所麻省理工学院

科学家

和微生物和细菌社区 cast 13

也与

引导 rna 绑定以检测病毒 rna

,一旦病毒 rna 被绑定 cast 13

开始一个称为侧链切割的过程

,这

意味着它会切断它检测到的任何 rna 片段

好吧,这似乎不是不必要的吗

?切割

随机 rna 片段对任何事情有什么作用?

令人惊讶的是,这是

夏洛克能力的核心,

所以 h Sherlock 是如何工作的,首先

研究人员采集了一个可能感染病毒的患者样本,

然后他们放大了

该样本中 rna 的水平,并添加了

对 cast 13 敏感的报告基因。接下来,将许多

工程 cast 13 添加到

样本中,并

带有 引导 rna 检测该病毒 rna

,一旦该病毒 rna 被绑定 cast 13

再次启动侧枝切割过程

意味着它会切断其路径中的任何东西,

包括报告者

以及为什么报告者

被清除是实际检测

到病毒的原因

记者有一个独特的标签,

当施法者团队将其一分为二时,

它们会产生一个独特的信号,可以

帮助检测

一个人是否感染了病毒,所以

想象一下

妊娠试验,

根据国家卫生服务局的说法,妊娠试验甚至可以做什么

怀孕的早期迹象是

身体在女性的血液和尿液中产生激素 hcg

或人类慢性促性腺激素

与经过特殊处理的条带接触,

测试检测是否

检测

到 hcg 现在这个

过程与切割的报告基因非常相似,

一旦报告基因被切片,他们就会像妊娠试验一样

进入商业流动检测系统

,以及

何时和 如果样本对该病毒呈阴性

则记者在第一条

检测线收集,但如果呈阳性,

他们将在不同的检测线收集,

从而很

容易发现诊断,就像

妊娠试验中

检测 covid19 的深红色和治疗线一样

正如我之前所说,正如

我现在所说的,

科学是惊人的,我们从一个

未知的无法识别的基因和一个随机

细菌开始,

并将其创造成一个经过认证的水果

忍者

战士 切水果 我们正在

切牛仔裤

发现是可能的 创新

总是在发生,解决方案总是

会发生 你可以被创造出来,所以让我们

回答那个学生的问题,

为什么科学家试图治愈罕见的

疾病而不是常见的疾病?

讲师应该说得好,

因为我们的世界充满了

有朝一日

能够治愈最致命的疾病的特性,

但在那之前 我们只需要等待,

所以时间是她问题的答案

,这也将是

我们大流行

的答案