4.6 Review Book Chapter

Viral Miniproteins

期刊

ANNUAL REVIEW OF MICROBIOLOGY, VOL 68
卷 68, 期 -, 页码 21-43

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-micro-091313-103727

关键词

transmembrane protein; traptamer; viroporin; hydrophobic; randomized library

资金

  1. NCI NIH HHS [R01 CA037157] Funding Source: Medline

向作者/读者索取更多资源

Many viruses encode short transmembrane proteins that play vital roles in virus replication or virulence. Because many of these proteins are less than 50 amino acids long and not homologous to cellular proteins, their open reading frames were often overlooked during the initial annotation of viral genomes. Some of these proteins oligomerize in membranes and form ion channels. Other miniproteins bind to cellular transmembrane proteins and modulate their activity, whereas still others have an unknown mechanism of action. Based on the underlying principles of transmembrane miniprotein structure, it is possible to build artificial small transmembrane proteins that modulate a variety of biological processes. These findings suggest that short transmembrane proteins provide a versatile mechanism to regulate a wide range of cellular activities, and we speculate that cells also express many similar proteins that have not yet been discovered.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据