通过结构导向衍生化发现强效麻疹病毒融合抑制肽。

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics MedChemComm Pub Date : 2025-01-24 DOI:10.1039/D4MD01006J
Ziwei Gao, Jiei Sasaki, Tateki Suzuki, Tomoaki Suzuki, Yuki Miwa, Shinsuke Sando, Takao Hashiguchi and Jumpei Morimoto
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引用次数: 0

摘要

融合抑制肽(FIP)是一种被称为麻疹病毒(MeV)感染抑制剂的短肽,可抑制麻疹病毒包膜与宿主细胞膜之间的膜融合。因此,FIP作为治疗MeV感染的候选药物是潜在的有用的,但抑制活性的改善是可取的。在这项研究中,我们进行了FIP的构效关系研究,并基于结果和先前报道的配合物的晶体结构,我们设计了FIP衍生物。从一系列衍生物中,我们发现了一个具有较强抑制活性(IC50 = 210 nM)的FIP衍生物,该衍生物与MeV融合蛋白的结合亲和力(K D = 6.6 nM)增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Discovery of potent measles virus fusion inhibitor peptides via structure-guided derivatization†

Fusion inhibitor peptide (FIP), a short peptide known as a measles virus (MeV) infection inhibitor, inhibits membrane fusion between the viral envelope of MeV and the host cell membrane. Therefore, FIP is potentially useful as a drug candidate for treating MeV infection, but improvement of inhibitory activity is desirable. In this study, we conducted a structure–activity relationship study of FIP and, based on the result and the previously reported crystal structure of the complex, we designed FIP derivatives. From a series of derivatives, we discovered an FIP derivative with a strong inhibitory activity (IC50 = 210 nM) derived from the enhanced binding affinity (KD = 6.6 nM) to the MeV fusion protein.

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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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