Evaluation of Phytopolyphenols for their gp120-CD4 Binding Inhibitory Properties by In Silico Molecular Modelling & In Vitro Cell Line Studies

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Author(s): Amit Mirani, Harish Kundaikar, Shilpa Velhal, Vainav Patel, Atmaram Bandivdekar, Mariam Degani, Vandana Patravale*.

Journal Name: Current HIV Research

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Abstract:

Background: Lack of effective early-stage HIV-1 inhibitor instigated the need for screening of novel gp120-CD4 binding inhibitor. Polyphenols, a secondary metabolite derived from natural sources are reported to have broad spectrum HIV-1 inhibitory activity. However, the gp120-CD4 binding inhibitory activity of polyphenols has not been analysed in silico yet.

Objectives: To establish the usage of phytopolyphenols (Theaflavin, Epigallocatechin (EGCG), Ellagic acid and Gallic acid) as early stage HIV-1 inhibitor by investigating their binding mode in reported homology of gp120-CD4 receptor complex using in silico screening studies and in vitro cell line studies.

Methods: The in silico molecular docking and molecular simulation studies were performed using Schrödinger 2013-2 suite installed on Fujitsu Celsius Workstation. The in vitro cell line studies were performed in the TZM-bl cell line using MTT assay and β-galactosidase assay.

Results: The results of molecular docking indicated that Theaflavin and EGCG exhibited high XP dock score with binding pose exhibiting van der Waals interaction and hydrophobic interaction at the deeper site in the Phe43 cavity with Asp368 and Trp427. Both Theaflavin and EGCG form a stable complex with the prepared HIV-1 receptor and their binding mode interaction are within the vicinity 4 Å. Further, in vitro cell line studies also confirmed that Theaflavin (SI= 252) and EGCG (SI= 138) exert better HIV-1 inhibitory activity as compared to Ellagic acid (SI= 30) and Gallic acid (SI=34).

Conclusions: The results elucidate possible binding mode of phytopolyphenols, which pinpoints their plausible mechanism and directs their usage as early stage HIV-1 inhibitor.

Keywords: In silico, Molecular docking, Theaflavin, EGCG, Ellagic acid, Gallic acid, gp120-CD4 binding inhibitor

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(E-pub Ahead of Print)
DOI: 10.2174/1570162X17666190611121627

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