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OALib Journal期刊
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Clustering of HIV-1 Subtypes Based on gp120 V3 Loop electrostatic properties

DOI: 10.1186/2046-1682-5-3

Keywords: HIV-1, protein-receptor interactions, Poisson-Boltzmann electrostatics, electrostatic similarity distance, electrostatic clustering

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Abstract:

Although the majority of consensus sequences have a net charge of +3, the spatial distribution of their electrostatic potentials and charges may be a discriminating factor for binding and infectivity. This is demonstrated by the formation of several small subclusters, within major clusters, which indicates common origin but distinct spatial details of electrostatic properties. Some of this information may be present, in a coarse manner, in clustering of sequences, but the spatial details are largely lost. We show the effect of ionic strength on clustering of electrostatic potentials, information that is not present in clustering of charges or sequences. We also make correlations between clustering of electrostatic potentials and net charge, coreceptor selectivity, global prevalence, and geographic distribution. Finally, we interpret coreceptor selectivity based on the N6X7T8|S8X9 sequence glycosylation motif, the specific positive charge location according to the 11/24/25 rule, and the overall charge and electrostatic potential distribution.We propose that in addition to the sequence and the net charge of the V3 loop of each subtype, the spatial distributions of electrostatic potentials and charges may also be important factors for receptor recognition and binding and subsequent viral entry into cells. This implies that the overall electrostatic potential is responsible for long-range recognition of the V3 loop with coreceptors CCR5/CXCR4, whereas the charge distribution contributes to the specific short-range interactions responsible for the formation of the bound complex. We also propose a scheme for coreceptor selectivity based on the sequence glycosylation motif, the 11/24/25 rule, and net charge.HIV-1 entry into the host cell is mediated by the viral envelope glycoprotein gp120 associated with gp41 and involves on the host cell surface the CD4 molecule together with the CCR5 or CXCR4 receptor [1,2]. Upon CD4 binding, a conformational change is induced in gp120,

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