On the cutting edge: protease-based methods for sensing and controlling cell biology

被引:32
作者
Chung, H. Kay [1 ,2 ,3 ,5 ]
Lin, Michael Z. [1 ,2 ,4 ]
机构
[1] Stanford Univ, Dept Neurobiol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Program Biol Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[5] Salk Inst Biol Studies, 10010 N Torrey Pines Rd, La Jolla, CA 92037 USA
关键词
VIRUS NS3/4A PROTEASE; NS2B-NS3; PROTEASE; CRYSTAL-STRUCTURE; IMMUNE-RESPONSES; SPLIT-UBIQUITIN; INHIBITOR; IDENTIFICATION; LIGHT; TANGO; SPECIFICITY;
D O I
10.1038/s41592-020-0891-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sequence-specific proteases have proven to be versatile building blocks for tools that report or control cellular function. Reporting methods link protease activity to biochemical signals, whereas control methods rely on engineering proteases to respond to exogenous inputs such as light or chemicals. In turn, proteases have inherent control abilities, as their native functions are to release, activate or destroy proteins by cleavage, with the irreversibility of proteolysis allowing sustained downstream effects. As a result, protease-based synthetic circuits have been created for diverse uses such as reporting cellular signaling, tuning protein expression, controlling viral replication and detecting cancer states. Here, we comprehensively review the development and application of protease-based methods for reporting and controlling cellular function in eukaryotes. This Review focuses on protease-based tools for sensing and controlling protein function in cell biology.
引用
收藏
页码:885 / 896
页数:12
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