Insights into effect of the Asp25/Asp25ʹ protonation states on binding of inhibitors Amprenavir and MKP97 to HIV-1 protease using molecular dynamics simulations and MM-GBSA calculations. Issue 8 (3rd August 2021)

• Record Type: Journal Article
• Authors: Yu, Y.X.; Wang, W.; Sun, H.B.; Zhang, L.L.; Wu, S.L.; Liu, W.T.
• Is Part Of: SAR and QSAR in environmental research. Volume 32:Issue 8(2021)
• Page Start: 615
• Page End: 641
• Publication Date: 2021-08-03
• Subjects: HIV-1 protease -- binding free energy -- protonation states -- molecular dynamics simulation -- MM-GBSA; Structure-activity relationships (Biochemistry) -- Periodicals; QSAR (Biochemistry) -- Periodicals; 572.4
• DOI: 10.1080/1062936X.2021.1939149
• Languages: English
• ISSNs: 1062-936X

Abstract

ABSTRACT: The protonation states of two aspartic acids in the catalytic strands of HIV-1 protease (PR) remarkably affect bindings of inhibitors to PR. It is requisite for the design of potent inhibitors towards PR to investigate the influences of Asp25/Asp25ʹ protonated states on dynamics behaviour of PR and binding mechanism of inhibitors to PR. In this work, molecular dynamics (MD) simulations, MM-GBSA method and principal component (PC) analysis were coupled to explore the effect of Asp25/Asp25′ protonation states on conformational changes of PR and bindings of Amprenavir and MKP97 to PR. The results show that the Asp25/Asp25′ protonation states exert different impacts on structural fluctuations, flexibility and motion modes of PR. Dynamics analysis verifies that Asp25/Asp25ʹ protonated states highly affect conformational dynamics of two flaps in PR. The binding free energy calculations results suggest that the Asp25/Asp25ʹ protonated states obviously strengthen bindings of inhibitors to PR compared to the non-protonation state. Calculations of residue-based free energy decomposition indicate that the Asp25/Asp25ʹ protonation not only disturbs the interaction network of inhibitors with PR but also stabilizes bindings of inhibitors to PR by cancelling the electrostatic repulsive interaction. Therefore, special attentions should be paid to the Asp25/Asp25ʹ protonation in the design of potent inhibitors towards PR.