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Biochem Biophys Res Commun. 2013 Jul 26;437(2):199-204. doi: 10.1016/j.bbrc.2013.06.027. Epub 2013 Jun 18.

Crystallographic study of multi-drug resistant HIV-1 protease lopinavir complex: mechanism of drug recognition and resistance.

Author information

1
Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, MI 48201, United States.

Abstract

Lopinavir (LPV) is a second generation HIV-1 protease inhibitor. Drug resistance has rapidly emerged against LPV since its US FDA approval on September 15, 2000. Mutations at residues 32I, L33F, 46I, 47A, I54V, V82A, I84V, and L90M render the protease drug resistant against LPV. We report the crystal structure of a clinical isolate multi-drug resistant (MDR) 769 HIV-1 protease (resistant mutations at residues 10, 36, 46, 54, 62, 63, 71, 82, 84, and 90) complexed with LPV and the in vitro enzymatic IC50 of LPV against MDR 769. The structural and functional studies demonstrate significant drug resistance of MDR 769 against LPV, arising from reduced interactions between LPV and the protease target.

KEYWORDS:

HAART; HIV-1 protease; IC50; LPV; Lopinavir; MDR; Multi-drug resistance; RMSD; X-ray crystallography; half maximal inhibitory concentration; highly active anti-retroviral therapy; lopinavir; multi-drug resistance; root mean square deviation

PMID:
23792096
PMCID:
PMC4520426
DOI:
10.1016/j.bbrc.2013.06.027
[Indexed for MEDLINE]
Free PMC Article

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