A Degraded Fragment of HIV-1 Gp120 in Rat Hepatocytes Forms Fibrils and Enhances HIV-1 Infection-Reference-Cited by-同舟云学术

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A Degraded Fragment of HIV-1 Gp120 in Rat Hepatocytes Forms Fibrils and Enhances HIV-1 Infection

Published:2017-10 Issue:7 Volume:113 Page:1425-1439
ISSN:0006-3495
Container-title:Biophysical Journal
language:en
Short-container-title:Biophysical Journal

Author:

Chen Jinquan,Ren Ruxia,Yu Fei,Wang Chunyan,Zhang Xuanxuan,Li Wenjuan,Tan Suiyi,Jiang Shibo,Liu Shuwen,Li Lin

Funder

Natural Science Foundation of China

Natural Science Fund for Colleges and Universities in Jiangsu Province

National S&T Key Special Foundation

Publisher

Elsevier BV

Subject

Biophysics

Reference49 articles.

1. Molecular mechanisms of HIV entry;Wilen;Adv. Exp. Med. Biol.,2012

2. HIV entry and its inhibition;Chan;Cell,1998

3. The current status and challenges in the development of fusion inhibitors as therapeutics for HIV-1 infection;Tan;Curr. Pharm. Des.,2013

4. Different from the HIV fusion inhibitor C34, the anti-HIV drug Fuzeon (T-20) inhibits HIV-1 entry by targeting multiple sites in gp41 and gp120;Liu;J. Biol. Chem.,2005

5. Peptides derived from HIV-1 gp120 co-receptor binding domain form amyloid fibrils and enhance HIV-1 infection;Tan;FEBS Lett.,2014

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3. CCR5 antagonist reduces HIV-induced amyloidogenesis, tau pathology, neurodegeneration, and blood-brain barrier alterations in HIV-infected hu-PBL-NSG mice;Molecular Neurodegeneration;2021-11-22

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