Protein-Protein Interactions in Transcription: A Fertile Ground for Helix Mimetics

被引:21
|
作者
Guarracino, Danielle A. [1 ]
Bullock, Brooke N. [1 ]
Arora, Paramjit S. [1 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
helix mimetics; protein-protein interactions; transcription; HYDROGEN-BOND-SURROGATE; BETA-PEPTIDE INHIBITORS; HIGH-AFFINITY LIGANDS; ALPHA-HELICES; TRANSACTIVATION DOMAIN; SELECTIVE INHIBITORS; P53-HDM2; INTERACTION; EFFICIENT SYNTHESIS; STRUCTURAL BASIS; DRUG DISCOVERY;
D O I
10.1002/bip.21546
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Designed ligands that inhibit protein-protein interactions involved in gene expression are valuable as reagents for genomics research and as leads for drug discovery efforts. Selective modulation of protein-protein interactions has proven to be a daunting task for synthetic ligands; however, the last decade has seen significant advances in inhibitor design, especially for helical protein interfaces. This review discusses examples of transcriptional complexes targeted by designer helices. (C) 2010 Wiley Periodicals, Inc. Biopolymers 95: 1-7, 2011.
引用
收藏
页码:1 / 7
页数:7
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