Engineering conditional protein-protein interactions for dynamic cellular control

被引:2
|
作者
Stohr, Anthony M. [1 ]
Ma, Derron [1 ]
Chen, Wilfred [1 ]
Blenner, Mark [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Dynamic regulation; Protein-protein interactions; Protein engineering; Computational protein design; SYSTEM; TOOL; TRANSCRIPTION; ORGANIZATION; DEGRADATION; CIRCUITS; COMPLEX; DESIGN; LOGIC;
D O I
10.1016/j.biotechadv.2024.108457
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Conditional protein-protein interactions enable dynamic regulation of cellular activity and are an attractive approach to probe native protein interactions, improve metabolic engineering of microbial factories, and develop smart therapeutics. Conditional protein-protein interactions have been engineered to respond to various chemical, light, and nucleic acid-based stimuli. These interactions have been applied to assemble protein fragments, build protein scaffolds, and spatially organize proteins in many microbial and higher-order hosts. To foster the development of novel conditional protein-protein interactions that respond to new inputs or can be utilized in alternative settings, we provide an overview of the process of designing new engineered protein interactions while showcasing many recently developed computational tools that may accelerate protein engineering in this space.
引用
收藏
页数:13
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