Thermodynamic Coupling Function Analysis of Allosteric Mechanisms in the Human Dopamine Transporter. Academic Article uri icon

Overview

abstract

  • Allostery plays a crucial role in the mechanism of neurotransmitter-sodium symporters, such as the human dopamine transporter. To investigate the molecular mechanism that couples the transport-associated inward release of the Na+ ion from the Na2 site to intracellular gating, we applied a combination of the thermodynamic coupling function (TCF) formalism and Markov state model analysis to a 50-μs data set of molecular dynamics trajectories of the human dopamine transporter, in which multiple spontaneous Na+ release events were observed. Our TCF approach reveals a complex landscape of thermodynamic coupling between Na+ release and inward-opening, and identifies diverse, yet well-defined roles for different Na+-coordinating residues. In particular, we identify a prominent role in the allosteric coupling for the Na+-coordinating residue D421, where mutation has previously been associated with neurological disorders. Our results highlight the power of the TCF analysis to elucidate the molecular mechanism of complex allosteric processes in large biomolecular systems.

publication date

  • November 15, 2017

Research

keywords

  • Dopamine Plasma Membrane Transport Proteins

Identity

PubMed Central ID

  • PMC5773750

Scopus Document Identifier

  • 85033778782

Digital Object Identifier (DOI)

  • 10.1016/j.bpj.2017.10.030

PubMed ID

  • 29153319

Additional Document Info

volume

  • 114

issue

  • 1