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Suppression of SARS-CoV entry by peptides corresponding to heptad regions on spike glycoprotein

Heptad repeat regions (HR1 and HR2) are highly conserved sequences located in the glycoproteins of enveloped viruses. They form a six-helix bundle structure and are important in the process of virus fusion. Peptides derived from the HR regions of some viruses have been shown to inhibit the entry of...

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Detalles Bibliográficos
Autores principales: Yuan, Kehu, Yi, Ling, Chen, Jian, Qu, Xiuxia, Qing, Tingting, Rao, Xi, Jiang, Pengfei, Hu, Jianhe, Xiong, Zikai, Nie, Yuchun, Shi, Xuanling, Wang, Wei, Ling, Chen, Yin, Xiaolei, Fan, Keqiang, Lai, Luhua, Ding, Mingxiao, Deng, Hongkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111000/
https://www.ncbi.nlm.nih.gov/pubmed/15184046
http://dx.doi.org/10.1016/j.bbrc.2004.05.046
Descripción
Sumario:Heptad repeat regions (HR1 and HR2) are highly conserved sequences located in the glycoproteins of enveloped viruses. They form a six-helix bundle structure and are important in the process of virus fusion. Peptides derived from the HR regions of some viruses have been shown to inhibit the entry of these viruses. SARS-CoV was also predicted to have HR1 and HR2 regions in the S2 protein. Based on this prediction, we designed 25 peptides and screened them using a HIV-luc/SARS pseudotyped virus assay. Two peptides, HR1-1 and HR2-18, were identified as potential inhibitors, with EC(50) values of 0.14 and 1.19 μM, respectively. The inhibitory effects of these peptides were validated by the wild-type SARS-CoV assay. HR1-1 and HR2-18 can serve as functional probes for dissecting the fusion mechanism of SARS-CoV and also provide the potential of further identifying potent inhibitors for SARS-CoV entry.