Engineering Allostery into Proteins

被引:11
|
作者
Gorman, Scott D. [1 ]
D'Amico, Rebecca N. [1 ]
Winston, Dennis S. [1 ]
Boehr, David D. [1 ]
机构
[1] Penn State Univ, Dept Chem, 152 Davey Lab, University Pk, PA 16802 USA
来源
关键词
Allostery; Protein regulation; Protein engineering; Energy landscape; Amino acid network; Domain insertion; Covalent modification; AMINO-ACID BIOSYNTHESIS; SYNERGISTIC ALLOSTERY; PHOTOCHROMIC AGONIST; DYNAMIC ALLOSTERY; STRUCTURAL BASIS; DNA-REPLICATION; GENE-REGULATION; DOMAIN; AZOBENZENE; BINDING;
D O I
10.1007/978-981-13-8719-7_15
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Our ability to engineer protein structure and function has grown dramatically over recent years. Perhaps the next level in protein design is to develop proteins whose function can be regulated in response to various stimuli, including ligand binding, pH changes, and light. Endeavors toward these goals have tested and expanded on our understanding of protein function and allosteric regulation. In this chapter, we provide examples from different methods for developing new allosterically regulated proteins. These methods range from whole insertion of regulatory domains into new host proteins, to covalent attachment of photoswitches to generate light-responsive proteins, and to targeted changes to specific amino acid residues, especially to residues identified to be important for relaying allosteric information across the protein framework. Many of the examples we discuss have already found practical use in medical and biotechnology applications.
引用
收藏
页码:359 / 384
页数:26
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