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Thermodynamic Coupling Function Analysis of Allosteric Mechanisms in the Human Dopamine Transporter
- Source :
- Biophysical Journal. 114:10-14
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
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.
- Subjects :
- Models, Molecular
0301 basic medicine
Protein Conformation
Stereochemistry
Allosteric regulation
Biophysics
Gating
03 medical and health sciences
Molecular dynamics
0302 clinical medicine
Allosteric Regulation
Animals
Humans
Dopamine transporter
State model
Dopamine Plasma Membrane Transport Proteins
biology
Biophysical Letter
Chemistry
Sodium
Function analysis
030104 developmental biology
Symporter
biology.protein
Thermodynamics
030217 neurology & neurosurgery
Intracellular
Subjects
Details
- ISSN :
- 00063495
- Volume :
- 114
- Database :
- OpenAIRE
- Journal :
- Biophysical Journal
- Accession number :
- edsair.doi.dedup.....861e95a9fb4691d65517e20c88a5b1d0
- Full Text :
- https://doi.org/10.1016/j.bpj.2017.10.030