Miniproteins as a Powerful Modality in Drug Development

被引:46
作者
Crook, Zachary R. [1 ]
Nairn, Natalie W. [2 ]
Olson, James M. [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, 1100 Fairview Ave N,Room 04-100, Seattle, WA 98109 USA
[2] Blaze Biosci Inc, 530 Fairview Ave N,Suite 1400, Seattle, WA 98109 USA
基金
美国国家卫生研究院;
关键词
AMINO-ACID; PEPTIDE; PROTEIN; DESIGN; INHIBITORS; DISCOVERY; CANCER; POTENT; PHARMACOLOGY; PENETRATION;
D O I
10.1016/j.tibs.2019.12.008
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
Miniproteins are a diverse group of protein scaffolds characterized by small (1-10 kDa) size, stability, and versatility in drug-like roles. Coming largely from native sources, they have been widely adopted into drug development pipelines. While their structures and capabilities are diverse, the approaches to their utilization share more similarities with each other than with more widely used modalities (e.g., antibodies or small molecules). In this review, we highlight recent advances in miniprotein-based approaches to otherwise poorly addressed clinical needs, including structure-based and functional characterization. We also summarize their unique screening strategies and pharmacology considerations. Through a greater understanding of the unique properties that make them attractive for drug design, miniproteins can be effectively utilized against targets that are intractable by other approaches.
引用
收藏
页码:332 / 346
页数:15
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