Author:

Keywords:

hiv-1 integrase, strand transfer, pi electron orbital interaction, immunodeficiency-virus type-1, protein-protein interactions, amino-acid-residues, functions in-vitro, reverse transcription, quantitative assay, coactivator p75, binding domain, identification, mutagenesis, Science & Technology, Life Sciences & Biomedicine, Virology, HIV-1 integrase, IMMUNODEFICIENCY-VIRUS TYPE-1, PROTEIN-PROTEIN INTERACTIONS, AMINO-ACID-RESIDUES, FUNCTIONS IN-VITRO, REVERSE TRANSCRIPTION, QUANTITATIVE ASSAY, COACTIVATOR P75, BINDING DOMAIN, IDENTIFICATION, MUTAGENESIS, DNA, Viral, Dimerization, Electrons, HIV Integrase, HIV-1, Humans, Virus Integration, 06 Biological Sciences, 07 Agricultural and Veterinary Sciences, 11 Medical and Health Sciences, 30 Agricultural, veterinary and food sciences, 31 Biological sciences, 32 Biomedical and clinical sciences

Abstract:

HIV-1 integrase (IN) is an essential enzyme for viral infection. Here, we report an extensive pi electron orbital interaction between four amino acids, W132, M178, F181 and F185, located at the dimeric interface of IN that is critical for the strand transfer activity alone. Catalysis of nine different mutant IN proteins at these positions were evaluated. Whereas the 3'-processing activity is predominantly strong, the strand transfer activity of each enzyme was completely dependent on an intact pi electron orbital interaction at the dimeric interface. Four representative IN mutants were constructed in the context of the infectious NL4.3 HIV-1 viral clone. Whereas viruses with an intact pi electron orbital interaction at the IN dimeric interface replicated comparable to wild type, viruses containing an abolished pi interaction were non-infectious. Q-PCR analysis of viral DNA forms during viral replication revealed pleiotropic effects of most mutations. We hypothesize that the pi interaction is a critical contact point for the assembly of functional IN multimeric complexes, and that IN multimerization is required for a functional pre-integration complex. The rational design of small molecule inhibitors targeting the disruption of this pi-pi interaction should lead to powerful anti-retroviral drugs. (C) 2008 Elsevier Inc. All rights reserved.