Targeting HIV-1 Protease Autoprocessing for High-throughput Drug Discovery and Drug Resistance Assessment-Reference-Cited by-同舟云学术

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Targeting HIV-1 Protease Autoprocessing for High-throughput Drug Discovery and Drug Resistance Assessment

Published:2019-01-22 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Huang Liangqun,Li Linfeng,Tien ChihFeng,LaBarbera Daniel V.,Chen Chaoping

Funder

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-36730-4.pdf

Reference51 articles.

1. Chen, J. et al. Cytoplasmic HIV-1 RNA is mainly transported by diffusion in the presence or absence of Gag protein. Proc Natl Acad Sci USA 111, E5205–5213 (2014).

2. Chen, C. & Montelaro, R. C. Characterization of RNA elements that regulate gag-pol ribosomal frameshifting in equine infectious anemia virus. J Virol 77, 10280–10287 (2003).

3. Huang, L. & Chen, C. Understanding HIV-1 protease autoprocessing for novel therapeutic development. Future Med Chem 5, 1215–1229 (2013).

4. Zybarth, G. & Carter, C. Domains upstream of the protease (PR) in human immunodeficiency virus type 1 Gag-Pol influence PR autoprocessing. J Virol 69, 3878 (1995).

5. Louis, J. M., Weber, I. T., Tozser, J., Clore, G. M. & Gronenborn, A. M. HIV-1 protease: maturation, enzyme specificity, and drug resistance. Adv Pharmacol 49, 111–146 (2000).

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