Theoretical investigation of the interactions in binding pocket of Reverse Transcriptase

Kamlesh Kumar Sahu, Nozomu Hatakeyama, Akira Miyamoto

Research output: Contribution to journalArticlepeer-review

Abstract

Interactions in proteins have been studied using several chemical information techniques including quantum chemical methods that are applied to truncated systems composed of the ligand molecule and the surrounding amino acids of the receptor. In this work we adopt an approach to study these interactions accounting for as many as possible explicit solvent molecules and without the need of a fragmented calculation. Furthermore, we embed our quantum chemical calculations within a molecular dynamics framework that enables a fundamentally fast system for quantum molecular dynamic simulations (QCMD). Central to this new system for QCMD is the tight binding QC system, newly developed in our laboratories, and which combined with the MD paradigm results in an ultra accelerated QCMD method for protein-ligand interaction evaluations. We have applied our newly developed method to the Nevirapine (NVP)-Reverse Transcriptase (RT) system. We show how the proposed method leads us to new findings. The advanced QCMD was applied to a system of RT with NVP and it has led to the knowledge of specific groups and atoms that interact with surrounding amino acids of RT and help in drug binding. The information derived from this calculation may be used in designing drugs for NVP resistant virus strains that have binding capability like NVP.

Original languageEnglish
Pages (from-to)719-724
Number of pages6
JournalSaudi Journal of Biological Sciences
Volume22
Issue number6
DOIs
Publication statusPublished - 2015 Nov 1

Keywords

  • Density function theory
  • Enzyme
  • Nevirapine
  • Quantum chemical molecular dynamics (QCMD) calculation
  • Reverse Transcriptase

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)

Fingerprint Dive into the research topics of 'Theoretical investigation of the interactions in binding pocket of Reverse Transcriptase'. Together they form a unique fingerprint.

Cite this