Border Crossings: Colicins and Transporters

被引:48
作者
Jakes, Karen S. [1 ]
Cramer, William A. [2 ]
机构
[1] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
来源
ANNUAL REVIEW OF GENETICS, VOL 46 | 2012年 / 46卷
关键词
outer membrane receptor; outer membrane translocator; PROTEIN-PROTEIN INTERACTIONS; OUTER-MEMBRANE TRANSPORT; CHANNEL-FORMING DOMAIN; N-TERMINAL DOMAIN; ESCHERICHIA-COLI; IMMUNITY PROTEIN; CRYSTAL-STRUCTURE; TRANSLOCATION DOMAIN; INNER MEMBRANE; R-DOMAIN;
D O I
10.1146/annurev-genet-110711-155427
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Colicins are protein toxins produced by Escherichia coli to kill related bacteria. They must cross the target cell outer membrane (OM), and some must also cross the inner membrane (IM). To accomplish cellular import, colicins have parasitized E. coli nutrient transporters as well as IM and periplasmic proteins normally used to maintain cell wall integrity or provide energy for nutrient uptake through transporters. Colicins have evolved to use both transporters and other membrane proteins through mechanisms different from those employed in physiological substrate uptake. Extended receptor-binding domains allow some colicins to search by lateral diffusion for binding sites on their OM translocators while bound to their primary OM receptor. Transport across the OM is initiated by entry of the unstructured N-terminal translocation domain into the translocator. Periplasmic and IM networks subsequently accomplish insertion of the colicin cytotoxic domain into or across the IM.
引用
收藏
页码:209 / 231
页数:23
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