Identification of Compounds Targeting Hepatitis B Virus Core Protein Dimerization through a Split Luciferase Complementation Assay

Author:

Wei Xia-Fei12,Gan Chun-Yang1,Cui Jing1,Luo Ying-Ying1,Cai Xue-Fei1,Yuan Yi1,Shen Jing1,Li Zhi-Ying1,Zhang Wen-Lu1,Long Quan-Xin1,Hu Yuan1,Chen Juan1,Tang Ni1,Guo Haitao3,Huang Ai-Long12,Hu Jie-Li12

Affiliation:

1. Key Laboratory of Molecular Biology on Infectious Diseases of the Ministry of Education, Department of Infectious Diseases, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China

2. Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases (CCID), Hangzhou, China

3. Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA

Abstract

The capsid of the hepatitis B virus is an attractive antiviral target for developing therapies against chronic hepatitis B infection. Currently available core protein allosteric modulators (CpAMs) mainly affect one of the two major types of protein-protein interactions involved in the process of capsid assembly, namely, the interaction between the core dimers.

Funder

Chongqing Education Commission

HHS | National Institutes of Health

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Chongqing Science and Technology Commission

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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