Molecular dynamics simulations to the bidirectional adhesion signaling pathway of integrin αV β3

Proteins. 2020 May;88(5):679-688. doi: 10.1002/prot.25849. Epub 2019 Nov 18.

Abstract

The bidirectional force transmission process of integrin through the cell membrane is still not well understood. Several possible mechanisms have been discussed in literature on the basis of experimental data, and in this study, we investigate these mechanisms by free and steered molecular dynamics simulations. For the first time, constant velocity pulling on the complete integrin molecule inside a dipalmitoyl-phosphatidylcholine membrane is conducted. From the results, the most likely mechanism for inside-out and outside-in signaling is the switchblade model with further separation of the transmembrane helices.

Keywords: dihedral principal component analysis; extracellular matrix; membrane protein; steered molecular dynamics; talin.

MeSH terms

  • 1,2-Dipalmitoylphosphatidylcholine / chemistry*
  • 1,2-Dipalmitoylphosphatidylcholine / metabolism
  • Binding Sites
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Crystallography, X-Ray
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / metabolism
  • Humans
  • Integrin alphaVbeta3 / chemistry*
  • Integrin alphaVbeta3 / genetics
  • Integrin alphaVbeta3 / metabolism
  • Molecular Dynamics Simulation
  • Principal Component Analysis
  • Protein Binding
  • Protein Conformation, alpha-Helical
  • Protein Conformation, beta-Strand
  • Protein Interaction Domains and Motifs
  • Thermodynamics

Substances

  • Integrin alphaVbeta3
  • 1,2-Dipalmitoylphosphatidylcholine