Rational design of small-molecule responsive protein switches

被引:2
|
作者
Shui, Sailan [1 ,2 ]
Buckley, Stephen [1 ,2 ]
Scheller, Leo [1 ,2 ]
Correia, Bruno E. [1 ,2 ]
机构
[1] Ecole Polytech Fed Lausanne, STI, Lab Prot Design & Immunoengn LPDI, Lausanne, Switzerland
[2] Swiss Inst Bioinformat SIB, Lausanne, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
computational protein design; protein switches; protein-ligand interactions; protein-protein interactions; small molecule; synthetic biology; INDUCED DIMERIZATION; BINDING DOMAIN; ACTIVATION; RAPAMYCIN; HAPTEN;
D O I
10.1002/pro.4774
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small-molecule responsive protein switches are powerful tools for controlling cellular processes. These switches are designed to respond rapidly and specifically to their inducer. They have been used in numerous applications, including the regulation of gene expression, post-translational protein modification, and signal transduction. Typically, small-molecule responsive protein switches consist of two proteins that interact with each other in the presence or absence of a small molecule. Recent advances in computational protein design already contributed to the development of protein switches with an expanded range of small-molecule inducers and increasingly sophisticated switch mechanisms. Further progress in the engineering of small-molecule responsive switches is fueled by cutting-edge computational design approaches, which will enable more complex and precise control over cellular processes and advance synthetic biology applications in biotechnology and medicine. Here, we discuss recent milestones and how technological advances are impacting the development of chemical switches.
引用
收藏
页数:12
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