Assessing Helical Protein Interfaces for Inhibitor Design

被引:230
作者
Bullock, Brooke N. [1 ]
Jochim, Andrea L. [1 ]
Arora, Paramjit S. [1 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
HOT-SPOTS; BINDING-ENERGY; FOLDAMERS; PEPTIDES; TARGETS;
D O I
10.1021/ja206074j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structure-based design of synthetic inhibitors of protein protein interactions (PPIs) requires adept molecular design and synthesis strategies as well as knowledge of targetable complexes. To address the significant gap between the elegant design of helix mimetics and their sporadic use in biology, we analyzed the full set of helical protein interfaces in the Protein Data Bank to obtain a snapshot of how helices that are critical for complex formation interact with the partner proteins. The results of this study are expected to guide the systematic design of synthetic inhibitors of PPIs. We have experimentally evaluated new classes of protein complexes that emerged from this data set, highlighting the significance of the results described herein.
引用
收藏
页码:14220 / 14223
页数:4
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