Gao Ziwei, Sasaki Jiei, Suzuki Tateki, Suzuki Tomoaki, Miwa Yuki, Sando Shinsuke, Hashiguchi Takao, Morimoto Jumpei
Depratement of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo Tokyo 113-8656 Japan
Laboratory of Medical Virology, Institute for Life and Medical Sciences, Kyoto University Kyoto 606-8507 Japan
RSC Med Chem. 2025 Jan 24;16(4):1619-1625. doi: 10.1039/d4md01006j. eCollection 2025 Apr 16.
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 (IC = 210 nM) derived from the enhanced binding affinity ( = 6.6 nM) to the MeV fusion protein.
融合抑制肽(FIP)是一种已知的麻疹病毒(MeV)感染抑制剂短肽,可抑制MeV病毒包膜与宿主细胞膜之间的膜融合。因此,FIP作为治疗MeV感染的候选药物具有潜在用途,但需要提高其抑制活性。在本研究中,我们对FIP进行了构效关系研究,并根据研究结果和先前报道的复合物晶体结构设计了FIP衍生物。从一系列衍生物中,我们发现了一种对MeV融合蛋白具有增强结合亲和力(Kd = 6.6 nM)从而具有强抑制活性(IC50 = 210 nM)的FIP衍生物。