Suppr超能文献

为CRISPR筛选增添化学生物学元素。

Adding a Chemical Biology Twist to CRISPR Screening.

作者信息

Huang Shiying, Baskin Jeremy M

机构信息

Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853 USA.

Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853 USA.

出版信息

Isr J Chem. 2023 Feb;63(1-2). doi: 10.1002/ijch.202200056. Epub 2022 Oct 18.

Abstract

In less than a decade, CRISPR screening has revolutionized forward genetics and cell and molecular biology. Advances in screening technologies, including sgRNA libraries, Cas9-expressing cell lines, and streamlined sequencing pipelines, have democratized pooled CRISPR screens at genome-wide scale. Initially, many such screens were survival-based, identifying essential genes in physiological or perturbed processes. With the application of new chemical biology tools to CRISPR screening, the phenotypic space is no longer limited to live/dead selection or screening for levels of conventional fluorescent protein reporters. Further, the resolution has been increased from cell populations to single cells or even the subcellular level. We highlight advances in pooled CRISPR screening, powered by chemical biology, that have expanded phenotypic space, resolution, scope, and scalability as well as strengthened the CRISPR/Cas enzyme toolkit to enable biological hypothesis generation and discovery.

摘要

在不到十年的时间里,CRISPR筛选彻底改变了正向遗传学以及细胞与分子生物学。筛选技术的进步,包括sgRNA文库、表达Cas9的细胞系以及简化的测序流程,使得全基因组规模的CRISPR混合筛选变得更加普及。最初,许多此类筛选都是基于生存的,旨在识别生理过程或受干扰过程中的必需基因。随着新的化学生物学工具应用于CRISPR筛选,表型空间不再局限于活/死选择或对传统荧光蛋白报告基因水平的筛选。此外,分辨率已从细胞群体提高到单细胞甚至亚细胞水平。我们重点介绍了由化学生物学推动的CRISPR混合筛选的进展,这些进展扩大了表型空间、分辨率、范围和可扩展性,同时强化了CRISPR/Cas酶工具包,以促进生物学假设的提出和发现。

相似文献

1
Adding a Chemical Biology Twist to CRISPR Screening.为CRISPR筛选增添化学生物学元素。
Isr J Chem. 2023 Feb;63(1-2). doi: 10.1002/ijch.202200056. Epub 2022 Oct 18.
6
Pooled CRISPR Screens in Drosophila Cells.果蝇细胞中的汇集式CRISPR筛选
Curr Protoc Mol Biol. 2019 Dec;129(1):e111. doi: 10.1002/cpmb.111.
9
CRISPR/Cas-based customization of pooled CRISPR libraries.基于 CRISPR/Cas 的高通量 CRISPR 文库定制。
PLoS One. 2018 Jun 20;13(6):e0199473. doi: 10.1371/journal.pone.0199473. eCollection 2018.

引用本文的文献

2
Synthetic Lipid Biology.合成脂质生物学
Chem Rev. 2025 Feb 26;125(4):2502-2560. doi: 10.1021/acs.chemrev.4c00761. Epub 2025 Jan 13.

本文引用的文献

2
High-content CRISPR screening.高内涵CRISPR筛选
Nat Rev Methods Primers. 2022;2(1). doi: 10.1038/s43586-022-00098-7. Epub 2022 Feb 10.
4
The phenotypic landscape of essential human genes.必需人类基因的表型景观。
Cell. 2022 Nov 23;185(24):4634-4653.e22. doi: 10.1016/j.cell.2022.10.017. Epub 2022 Nov 7.
7
Roles of PIKfyve in multiple cellular pathways.PIKfyve 在多种细胞途径中的作用。
Curr Opin Cell Biol. 2022 Jun;76:102086. doi: 10.1016/j.ceb.2022.102086. Epub 2022 May 16.
10
Saturation variant interpretation using CRISPR prime editing.使用 CRISPR 先导编辑进行饱和变异解读。
Nat Biotechnol. 2022 Jun;40(6):885-895. doi: 10.1038/s41587-021-01201-1. Epub 2022 Feb 21.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验