中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Viroporins beyond pathogenesis: Ion channel properties as the key to unlocking a neglected antiviral target

文献类型:期刊论文

作者Peng, Suya1,2; Wang, Yi1,2; Gao, Zhaobing1,2; Xia, Bingqing1,2
刊名PHARMACOLOGICAL RESEARCH
出版日期2025-09-01
卷号219页码:14
关键词Viroporins Ion selectivity Pathogenic mechanism Anti-viral drug discovery
ISSN号1043-6618
DOI10.1016/j.phrs.2025.107863
英文摘要A class of proteins encoded by viral genomes, referred to as viroporins, is composed of small hydrophobic proteins that form pores or ion channels in host membranes. These proteins modulate the viral life cycle and pathogenicity. Despite their early discovery and functional significance, viroporins have long remained underexploited as antiviral drug targets-partly due to the emergence of alternative antiviral strategies, viral evolutionary complexity, and technical limitations in studying channel function. Nonetheless, accumulating evidence underscores their essential roles in pathogenesis and viral fitness, positioning them as promising but underdeveloped therapeutic targets. While recent reviews have revisited the field, most have focused on the pathological functions of viroporins, with little attention given to the fundamental biophysical properties that define them as ion channels. Given that channel function is intrinsically governed by attributes such as ion selectivity and gating mechanisms, a mechanistic understanding of these properties is critical for understanding the pathogenic mechanism and rational drug development. To our knowledge, no prior review has systematically addressed viroporins from a channel-centric perspective. Here, we propose a reclassification framework grounded in the core biophysical attributes of viral channels, highlighting their ion permeability, gating behavior, and regulatory features. By shifting the focus from pathophysiology to channel function, this work aims to provide a conceptual foundation for future antiviral strategies and to stimulate broader interest in this underexplored but compelling class of viral targets.
WOS关键词HEPATITIS-C-VIRUS ; SMALL HYDROPHOBIC PROTEIN ; VIRAL-PROTEINS ; PROTON CHANNEL ; VPU PROTEIN ; 6K PROTEIN ; P7 ; MECHANISM ; FORMS ; SELECTIVITY
资助项目National Natural Science Foundation of China[92169202] ; National Natural Science Foundation of China[82341058] ; National Natural Science Foundation of China[82202491] ; National Natural Science Foundation of China[82394463] ; Chinese Academy of Sciences[PTYQ2024YZ0008] ; Shanghai Municipal Science and Technology Major Project[23JC1404301]
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:001540626100001
出版者ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/321156]  
专题国家级研究中心_原创新药研究全国重点实验室
通讯作者Gao, Zhaobing; Xia, Bingqing
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
2.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
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GB/T 7714
Peng, Suya,Wang, Yi,Gao, Zhaobing,et al. Viroporins beyond pathogenesis: Ion channel properties as the key to unlocking a neglected antiviral target[J]. PHARMACOLOGICAL RESEARCH,2025,219:14.
APA Peng, Suya,Wang, Yi,Gao, Zhaobing,&Xia, Bingqing.(2025).Viroporins beyond pathogenesis: Ion channel properties as the key to unlocking a neglected antiviral target.PHARMACOLOGICAL RESEARCH,219,14.
MLA Peng, Suya,et al."Viroporins beyond pathogenesis: Ion channel properties as the key to unlocking a neglected antiviral target".PHARMACOLOGICAL RESEARCH 219(2025):14.

入库方式: OAI收割

来源:上海药物研究所

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