生物
联动装置(软件)
遗传学
计算生物学
细胞生物学
进化生物学
基因
作者
Christian Renz,Evrydiki Asimaki,Cindy Meister,Véronique Albanèse,Kirill Petriukov,Nils Krapoth,Sabrina Wegmann,Hans-Peter Wollscheid,Ronald P.C. Wong,Amit Fulzele,Jia‐Xuan Chen,Sébastien Léon,Helle D. Ulrich
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2023-12-15
卷期号:84 (2): 386-400.e11
被引量:2
标识
DOI:10.1016/j.molcel.2023.11.016
摘要
The posttranslational modifier ubiquitin regulates most cellular processes. Its ability to form polymeric chains of distinct linkages is key to its diverse functionality. Yet, we still lack the experimental tools to induce linkage-specific polyubiquitylation of a protein of interest in cells. Here, we introduce a set of engineered ubiquitin protein ligases and matching ubiquitin acceptor tags for the rapid, inducible linear (M1-), K48-, or K63-linked polyubiquitylation of proteins in yeast and mammalian cells. By applying the so-called "Ubiquiton" system to proteasomal targeting and the endocytic pathway, we validate this tool for soluble cytoplasmic and nuclear as well as chromatin-associated and integral membrane proteins and demonstrate how it can be used to control the localization and stability of its targets. We expect that the Ubiquiton system will serve as a versatile, broadly applicable research tool to explore the signaling functions of polyubiquitin chains in many biological contexts.
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