Protocol for CRISPR-based endogenous protein tagging in mammalian cells

被引：1

作者：

Xiao, Yu-Xi ^{[1
,2
]}

Wei, Jiarun ^{[1
,2
]}

Moffat, Jason ^{[1
,2
,3
]}

机构：

[1] Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada

[2] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada

[3] Univ Toronto, Inst Biomed Engn, Toronto, ON, Canada

来源：

STAR PROTOCOLS | 2024年 / 5卷 / 04期

关键词：

NA expression vector; Steps for lipid; mammalian cells; ENDONUCLEASE;

D O I：

10.1016/j.xpro.2024.103404

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

Tracking the localization and proximal interaction partners of endogenous proteins provides valuable functional insight. Here, we present a protocol for CRISPR-based endogenous protein tagging in mammalian cells. We describe steps for endogenously tagging human TSC22D2 and MAP4, including designing Cas9 and Cas12a guides for knockin, modularized repair template design and cloning, and procedures for lipid transfection and electroporation. This protocol accommodates Cas nucleases in plasmid expression or ribonucleoprotein complex (RNP) formats. This "endo-tagging"approach offers flexibility and broad applicability. For complete details on the use and execution of this protocol, please refer to Xiao et al.1

引用

页数：25

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