Structure and Dynamics Study of LeuT Using the Markov State Model and Perturbation Response Scanning Reveals Distinct Ion Induced Conformational States

• Published in: The journal of physical chemistry. B 2016-08, Vol.120 (33), p.8361-8368
• Main Authors: Asciutto, Eliana K, Gedeon, Patrick C, General, Ignacio J, Madura, Jeffry D
• Format: Article
• Language: English
• Subjects: Amino Acid Transport Systems, Neutral - metabolism; Bacteria; Bacterial Proteins - metabolism; Computer Simulation; Ions - metabolism; Markov Chains; Models, Molecular; Protein Conformation; Sodium - metabolism
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/acs.jpcb.6b02053

The bacterial leucine transporter (LeuT), a close homologue of the eukaryote monoamine transporters (MATs), currently serves as a powerful template for computer simulations of MATs. Transport of the amino acid leucine through the membrane is made possible by the sodium electrochemical potential. Recent reports indicate that the substrate transport mechanism is based on structural changes such as hinge movements of key transmembrane domains. In order to further investigate the role of sodium ions in the uptake of leucine, here we present a Markov state model analysis of atomistic simulations of lipid embedded LeuT in different environments, generated by varying the presence of binding pocket sodium ions and substrate. Six metastable conformations are found, and structural differences between them along with transition probabilities are determined. We complete the analysis with the implementation of perturbation response scanning on our system, determining the most sensitive and influential regions of LeuT, in each environment. Our results show that the occupation of sites Na1 and Na2, along with the presence of the substrate, selectively influences the geometry of LeuT. In particular, the occupation of each site Na1/Na2 has strong effects (in terms of changes in influence and/or sensitivity, as compared to the case without ions) in specific regions of LeuT, and the effects are different for simultaneous occupation. Our results strengthen the rationale and provide a conformational mechanism for a putative transport mechanism in which Na2 is necessary, but may not be sufficient, to initiate and stabilize extracellular substrate access to the binding pocket.