Mechanistic insights of CRISPR/Cas nucleases for programmable targeting and early-stage diagnosis: A review

清脆的 计算生物学 计算机科学 反式激活crRNA 分子诊断学 纳米技术 核酸检测 Cas9 核酸 生物 生物信息学 遗传学 材料科学 基因
作者
Jean de Dieu Habimana,Rongqi Huang,Bertrand Muhoza,Ndayambaje Yvan Kalisa,Xiaobo Han,Weiyue Deng,Zhiyuan Li
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:203: 114033-114033 被引量:40
标识
DOI:10.1016/j.bios.2022.114033
摘要

Conventional and routine diagnostics such as polymerase chain reaction (PCR) and serological tests are less sensitive, costly, and require sample pretreatment procedures. CRISPR/Cas systems that inherently assist bacteria and archaea in destroying invading phage genetic materials via an RNA-mediated interference strategy have been reconstituted in vitro and harnessed for nucleic and non-nucleic acid diagnostics. CRISPR/Cas-based diagnostics (CRISPR-Dx) are cost-effective, possess excellent sensitivity (attomolar) and specificity (single base distinction), exhibit fast turnaround response, and support nucleic acid extraction-free workflow. However, CRISPR-Dx still needs to address various challenges to translate the laboratory work into end-user tailored solutions. In this perspective, we review the relevant progress of CRISPR/Cas systems-based diagnostics, focusing on the comprehensive customization and applications of leading and trending CRISPR/Cas systems as platform technologies for fluorescence, colorimetric, and electrical signal detection. The impact of the CRISPR game-changing technology on the COVID-19 pandemic is highlighted. We also demonstrate the role of CRISPR/Cas systems for carryover contamination prevention. The advancements in signal amplification strategies using engineered crRNAs, novel reporters, nanoparticles, artificial genetic circuits, microfluidics, and smartphones are also covered. Furthermore, we critically discuss the translation of CRISPR-Dx's basic research into end-user diagnostics for commercialization success in the near future. Finally, we discuss the complex challenges and alternative solutions to harness the CRISPR/Cas potential in detail.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
笑点低蜜蜂完成签到,获得积分10
刚刚
ttong完成签到,获得积分10
刚刚
silk发布了新的文献求助30
1秒前
今后应助aiyowei采纳,获得10
1秒前
orixero应助YangSY采纳,获得10
1秒前
2秒前
时光不染完成签到,获得积分10
2秒前
ckbadwny完成签到,获得积分10
2秒前
一抹晨曦完成签到,获得积分10
2秒前
名侦探柯基完成签到 ,获得积分10
2秒前
黄莉雯完成签到,获得积分20
2秒前
今后应助SYSUer采纳,获得10
3秒前
搜集达人应助75986686采纳,获得10
3秒前
梦泊完成签到 ,获得积分10
3秒前
李颜龙完成签到,获得积分10
4秒前
海蓝云天应助Shenmm采纳,获得10
4秒前
小王发布了新的文献求助10
4秒前
可爱的函函应助阳光念桃采纳,获得100
4秒前
共享精神应助heeu采纳,获得10
5秒前
5秒前
Hello应助ZNan采纳,获得10
5秒前
5秒前
苏11完成签到,获得积分10
6秒前
6秒前
菠萝完成签到,获得积分10
7秒前
田様应助Heisenberg采纳,获得10
7秒前
7秒前
7秒前
努力码字的上进小姐妹加油完成签到,获得积分0
7秒前
年轻的凤完成签到,获得积分10
7秒前
Khuram应助lamer采纳,获得10
7秒前
我是老大应助化雪彼岸采纳,获得10
7秒前
xie完成签到,获得积分10
7秒前
8秒前
9秒前
March完成签到,获得积分10
9秒前
Twonej应助大力日记本采纳,获得200
9秒前
9秒前
哎呀完成签到,获得积分10
9秒前
文昌鱼不是鱼完成签到 ,获得积分10
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Principles of town planning : translating concepts to applications 500
Short-Wavelength Infrared Windows for Biomedical Applications 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6059838
求助须知:如何正确求助?哪些是违规求助? 7892429
关于积分的说明 16301140
捐赠科研通 5204106
什么是DOI,文献DOI怎么找? 2784154
邀请新用户注册赠送积分活动 1766872
关于科研通互助平台的介绍 1647244