Residue-specific free energy analysis in ligand bindings to JAK2

Yifan Zhou, Xiao Liu, Youzhi Zhang, Long Peng, John Z.H. Zhang

Research output: Contribution to journalArticlepeer-review

Abstract

Janus kinase 2 (JAK2) has vital importance on the regulation of proliferation, survival and differentiation of a variety of cells by the activation of JAK-STAT pathway. In this study, we employ a new approach to quantitatively calculate residue-specific binding free energies to identify hot-spots in ligand bindings to JAK2 using computational alanine scanning technique combined with the interaction entropy method for entropic change in binding free energies. This combined approach allows one to quantitatively analyse important protein–ligand binding interactions, and in addition, provides a new method for more accurate computation of total protein–ligand binding free energy. In this report, we computed a total of 14 JAK2–ligand binding systems, all with crystal structures and experimentally measured binding data. Key residues are identified with L983 being the quantitatively dominant residue in binding free energy contributions to the ligands. The values of the computed total JAK2–ligand binding free energies are in much closer agreement with experimentally measured data than those obtained by using the standard MM/GBSA approach. Our study thus provided new insights into specific binding mechanisms in ligand binding to JAK2.

Original languageEnglish (US)
Pages (from-to)2633-2641
Number of pages9
JournalMolecular Physics
Volume116
Issue number19-20
DOIs
StatePublished - Oct 18 2018

Keywords

  • JAK2
  • MD simulation
  • MM/GBSA
  • Residue-specific
  • alanine scanning
  • binding free energy
  • interaction entropy

ASJC Scopus subject areas

  • Biophysics
  • Molecular Biology
  • Condensed Matter Physics
  • Physical and Theoretical Chemistry

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