Molecular dynamics study on folding and allostery in RfaH

Proteins. 2015 Sep;83(9):1582-92. doi: 10.1002/prot.24839. Epub 2015 Jul 20.

Abstract

Upon being released from the N-terminal domain (NTD), the C-terminal domain (CTD) switches from α-helix conformation to β-barrel conformation, which converts RfaH from a transcription factor into an activator of translation. The α→β conformational change may be viewed as allosteric transition. We use molecular dynamics simulations of coarse-grained off-lattice model to study the thermal folding of NTD, CTD, RfaH and the allosteric transition in CTD. The melting temperatures from the specific heat profiles indicate that the β-barrel conformation is much more stable than the α-helix conformation. Two helices in α-helix conformation have similar thermodynamic stabilities and the melting temperatures for β sheets show slight dispersion. Under the interaction with NTD, CTD is greatly stabilized and the cooperativity for thermal folding is also significantly improved. The α→β allosteric transition can be approximately described by a two-state model and three parallel pathways are identified. The transition state ensemble, quantified by a Tanford β-like parameter, resembles the α-helix and β-barrel conformations almost to the same extent.

Keywords: SOP-sidechain model; allostery; melting temperature; thermal folding; transition state ensemble.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Allosteric Regulation
  • Binding Sites
  • Escherichia coli Proteins / chemistry*
  • Kinetics
  • Molecular Dynamics Simulation*
  • Peptide Elongation Factors / chemistry*
  • Protein Binding
  • Protein Conformation*
  • Protein Folding*
  • Protein Stability
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Temperature
  • Thermodynamics
  • Trans-Activators / chemistry*

Substances

  • Escherichia coli Proteins
  • Peptide Elongation Factors
  • RfaH protein, E coli
  • Trans-Activators