Comparative molecular dynamics study of dimeric and monomeric forms of HIV-1 protease in ligand bound and unbound state

Rok, strany: 2017, 141 - 154

Human immunodeficiency virus type 1 protease is a viral-encoded enzyme and it is essential for replication and assembly of the virus. Inactivation of HIV-1 protease causes production of immature, noninfectious viral particles and thus HIV-1 protease is an attractive target in anti-AIDS drug design. In our current work, we performed molecular dynamics (MD) calculations (500 ns) for two different ligands (COM5 – designed in our previous study, and Darunavir) and made effort to understand dynamics behaviour of our designed compound COM5. An apo form of HIV-1 protease as monomer and dimer form was also studied in order to analyze response of protein to the ligand. MD results suggest that presence of ligand in hinders the stability of HIV-1 protease and one monomer from dimer systems is dominant on other monomer in terms of interaction made with ligands. We were able to trace functional residues as well as continuous motion of opening and closing (clapping) of flap region in HIV-1 protease (apo form) during entire 1000 ns of MD simulation. COM5 showed almost similar behaviour towards HIV-1 protease enzyme as Darunavir and propose as promising lead compound for the development of new inhibitor for HIV-1 protease.

ISO 690:

Padariya, M., Kalathiya, U. 2017. Comparative molecular dynamics study of dimeric and monomeric forms of HIV-1 protease in ligand bound and unbound state. In General Physiology and Biophysics, vol. 36, no.2, pp. 141-154. 0231-5882.

APA:

Padariya, M., Kalathiya, U. (2017). Comparative molecular dynamics study of dimeric and monomeric forms of HIV-1 protease in ligand bound and unbound state. General Physiology and Biophysics, 36(2), 141-154. 0231-5882.