| Literature DB >> 33734687 |
Suraj Makhija1, David Brown2, Rachel M Rudlaff2, Julia K Doh2, Struan Bourke2, Yina Wang2, Shuqin Zhou3,4, Rasmi Cheloor-Kovilakam2, Bo Huang2,5,6.
Abstract
Recent advances in genome engineering have expanded our capabilities to study proteins in their natural states. In particular, the ease and scalability of knocking-in small peptide tags has enabled high throughput tagging and analysis of endogenous proteins. To improve enrichment capacities and expand the functionality of knock-ins using short tags, we developed the tag-assisted split enzyme complementation (TASEC) approach, which uses two orthogonal small peptide tags and their cognate binders to conditionally drive complementation of a split enzyme upon labeled protein expression. Using this approach, we have engineered and optimized the tag-assisted split HaloTag complementation system (TA-splitHalo) and demonstrated its versatile applications in improving the efficiency of knock-in cell enrichment, detection of protein-protein interaction, and isolation of biallelic gene edited cells through multiplexing.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33734687 PMCID: PMC8115985 DOI: 10.1021/acschembio.0c00925
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100