Decrypting protein insertion through the translocon with free-energy calculations

Biochim Biophys Acta. 2016 Jul;1858(7 Pt B):1663-71. doi: 10.1016/j.bbamem.2016.02.017. Epub 2016 Feb 16.

Abstract

Protein insertion into a membrane is a complex process involving numerous players. The most prominent of these players is the Sec translocon complex, a conserved protein-conducting channel present in the cytoplasmic membrane of bacteria and the membrane of the endoplasmic reticulum in eukaryotes. The last decade has seen tremendous leaps forward in our understanding of how insertion is managed by the translocon and its partners, coming from atomic-detailed structures, innovative experiments, and well-designed simulations. In this review, we discuss how experiments and simulations, hand-in-hand, teased out the secrets of the translocon-facilitated membrane insertion process. In particular, we focus on the role of free-energy calculations in elucidating membrane insertion. Amazingly, despite all its apparent complexity, protein insertion into membranes is primarily driven by simple thermodynamic and kinetic principles. This article is part of a Special Issue entitled: Membrane proteins edited by J.C. Gumbart and Sergei Noskov.

Keywords: Free-energy calculations; Importance-sampling algorithms; Protein insertion; Sec translocon complex.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Algorithms
  • Binding Sites
  • Cell Membrane / chemistry*
  • Cell Membrane / ultrastructure*
  • Computer Simulation
  • Energy Transfer
  • Hydrophobic and Hydrophilic Interactions
  • Lipid Bilayers / chemistry*
  • Membrane Proteins / chemistry*
  • Membrane Proteins / ultrastructure*
  • Models, Chemical
  • Molecular Dynamics Simulation*
  • Protein Binding
  • Protein Conformation
  • Protein Interaction Mapping / methods
  • Thermodynamics

Substances

  • Lipid Bilayers
  • Membrane Proteins