Metals in Protein-Protein Interfaces

被引:62
作者
Song, Woon Ju [1 ]
Sontz, Pamela A. [1 ]
Ambroggio, Xavier I. [2 ]
Tezcan, F. Akif [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Rosetta Design Grp LLC, Burlington, VT 05401 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 43 | 2014年 / 43卷
基金
美国国家科学基金会;
关键词
metal/metallocofactors; protein-protein interactions; protein self-assembly; interfacial metal clusters; metal-mediated oligomerization; ZINC TRANSPORTER YIIP; CARBON-MONOXIDE DEHYDROGENASE; RAY CRYSTAL-STRUCTURE; HUMAN INSULIN HEXAMER; ALPHA-BETA-TUBULIN; STRUCTURAL BASIS; BINDING-SITE; METHANOSARCINA-THERMOPHILA; CRYSTALLOGRAPHIC EVIDENCE; RHODOSPIRILLUM-RUBRUM;
D O I
10.1146/annurev-biophys-051013-023038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
From the catalytic reactions that sustain the global oxygen, nitrogen, and carbon cycles to the stabilization of DNA processing proteins, transition metal ions and metallocofactors play key roles in biology. Although the exquisite interplay between metal ions and protein scaffolds has been studied extensively, the fact that the biological roles of the metals often stem from their placement in the interfaces between proteins and protein subunits is not always recognized. Interfacial metal ions stabilize permanent or transient protein-protein interactions, enable protein complexes involved in cellular signaling to adopt distinct conformations in response to environmental stimuli, and catalyze challenging chemical reactions that are uniquely performed by multisubunit protein complexes. This review provides a structural survey of transition metal ions and metallocofactors found in protein-protein interfaces, along with a series of selected examples that illustrate their diverse biological utility and significance.
引用
收藏
页码:409 / 431
页数:23
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