Bioorthogonal dissection of the replicase assembly of hepatitis C virus-Reference-Cited by-同舟云学术

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Bioorthogonal dissection of the replicase assembly of hepatitis C virus

Published:2021-09 Issue:9 Volume:28 Page:1366-1378.e4
ISSN:2451-9456
Container-title:Cell Chemical Biology
language:en
Short-container-title:Cell Chemical Biology

Author:

Zhang Yang,Chen Shuiye,Yuan Zhenghong,Yi Zhigang

Funder

National Major Science and Technology Projects of China

Rockefeller University

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,Biochemistry

Reference48 articles.

1. Helicase and capping enzyme active site mutations in brome mosaic virus protein 1a cause defects in template recruitment, negative-strand RNA synthesis, and viral RNA capping;Ahola;J. Virol.,2000

2. Essential role of domain III of nonstructural protein 5A for hepatitis C virus infectious particle assembly;Appel;PLoS Pathog.,2008

3. Identification and properties of the RNA-dependent RNA polymerase of hepatitis C virus;Behrens;EMBO J.,1996

4. Daclatasvir-like inhibitors of NS5A block early biogenesis of hepatitis C virus-induced membranous replication factories, independent of RNA replication;Berger;Gastroenterology,2014

5. Interaction between nonstructural proteins NS4B and NS5A is essential for proper NS5A localization and hepatitis C virus RNA replication;Biswas;J. Virol.,2016

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4. Identification and characterization of key residues in Zika virus envelope protein for virus assembly and entry;Emerging Microbes & Infections;2022-06-10

5. From Discovery to Cure, A Great Journey of the Hepatitis C Virus Study;Infectious Diseases & Immunity;2022-04

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