Suppr超能文献

严重急性呼吸综合征冠状病毒2 6-螺旋束融合核心与基于肽的融合抑制剂的结构与功能综述

Structure and Function of the SARS-CoV-2 6-HB Fusion Core and Peptide-Based Fusion Inhibitors: A Review.

作者信息

Liang Guodong, Li Yue, Li Ruijuan, Ma Yuheng, Na Heiya

机构信息

Key Laboratory for Candidate Drug Design and Screening Based on Chemical Biology, College of Pharmacy, Inner Mongolia Medical University, Huhhot, 010110, P.R. China.

Astbury Centre for Structural Molecular Biology, University of Leeds, Woodhouse Lane, LeedsLS2 9JT, UK.

出版信息

Curr Med Chem. 2023 Nov 24. doi: 10.2174/0109298673265694231113061842.

Abstract

SARS-CoV-2 has swept the world in recent years, triggering a global COVID-19 with a tremendous impact on human health and public safety. Similar to other coronaviruses, the six-helix bundle(6-HB) is not only a core structure driving the fusion of the SARS-CoV-2 envelope with the host cell membrane, but also the target of fusion inhibitors. The sequences from the HR1 or HR2 regions composing 6-HB are thus the original primary structures for the development of peptide-based fusion inhibitors. This review summarized the structure-activity relationship of the SARS-CoV-2 6- HB, analyzed the design methods and functional characteristics of peptide-based fusion inhibitors that contain different regions of HRs, and provided an outlook on the cutting- edge approaches for optimal modification of lead compounds (pan-coronavirization, chemical modification, superhelical construction, etc). We hope that this review will provide researchers with a comprehensive understanding of the state-of-art research progress on both 6-HB and peptide-based fusion inhibitors of SARS-CoV-2, and provide some new insights for the development of antiviral drugs.

摘要

近年来,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)席卷全球,引发了全球新冠肺炎疫情,对人类健康和公共安全造成了巨大影响。与其他冠状病毒类似,六螺旋束(6-HB)不仅是驱动SARS-CoV-2包膜与宿主细胞膜融合的核心结构,也是融合抑制剂的作用靶点。因此,构成6-HB的HR1或HR2区域的序列是开发基于肽的融合抑制剂的原始主要结构。本综述总结了SARS-CoV-2 6-HB的构效关系,分析了包含不同HR区域的基于肽的融合抑制剂的设计方法和功能特性,并对先导化合物的优化修饰前沿方法(泛冠状病毒化、化学修饰、超螺旋构建等)进行了展望。我们希望本综述能让研究人员全面了解SARS-CoV-2的6-HB和基于肽的融合抑制剂的最新研究进展,并为抗病毒药物的开发提供一些新的见解。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验