How protein engineering has revealed the molecular mechanisms of pore-forming toxins

被引:1
|
作者
Evans, Jordan C. [1 ]
Tweten, Rodney K. [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73190 USA
来源
PORE-FORMING TOXINS | 2021年 / 649卷
关键词
CHOLESTEROL-DEPENDENT CYTOLYSIN; STAPHYLOCOCCAL ALPHA-HEMOLYSIN; THIOL-ACTIVATED CYTOLYSIN; MEMBRANE-SPANNING DOMAIN; COLD DENATURATION; CRYSTAL-STRUCTURE; PREPORE COMPLEX; INSERTION; CHANNEL; OLIGOMERIZATION;
D O I
10.1016/bs.mie.2021.01.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pore-forming proteins are found in prokaryotes, vertebrates, and invertebrates, and when involved in pathogenic processes they are classified as pore-forming toxins (PFTs). The use of gene engineering methods in combination with the information provided by the high-resolution crystal structures of the PFTs have allowed investigators to gain a deep understanding of their pore-forming mechanisms. In this chapter, we discuss how protein engineering has helped us and others to reveal the molecular mechanisms of pore formation by prokaryotic PFTs with an emphasis on our experiences with the cholesterol-dependent cytolysins (CDCs).
引用
收藏
页码:47 / 70
页数:24
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