Thermodynamic Coupling Function Analysis of Allosteric Mechanisms in the Human Dopamine Transporter

被引:12
|
作者
LeVine, Michael V. [1 ,2 ]
Cuendet, Michel A. [1 ,2 ]
Razavi, Asghar M. [1 ]
Khelashvili, George [1 ,2 ]
Weinstein, Harel [1 ,2 ]
机构
[1] Cornell Univ, Dept Physiol & Biophys, Weill Cornell Med Coll, New York, NY 10021 USA
[2] Cornell Univ, HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsau, Weill Cornell Med Coll, New York, NY 10021 USA
关键词
NEUROTRANSMITTER-SODIUM SYMPORTER; CONFORMATIONAL DYNAMICS; SUBSTRATE; NA+; RELEASE;
D O I
10.1016/j.bpj.2017.10.030
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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-mu s 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.
引用
收藏
页码:10 / 14
页数:5
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