Conformational transitions of the sodium-dependent sugar transporter, vSGLT

Proc Natl Acad Sci U S A. 2018 Mar 20;115(12):E2742-E2751. doi: 10.1073/pnas.1718451115. Epub 2018 Mar 5.

Abstract

Sodium-dependent transporters couple the flow of Na+ ions down their electrochemical potential gradient to the uphill transport of various ligands. Many of these transporters share a common core structure composed of a five-helix inverted repeat and deliver their cargo utilizing an alternating-access mechanism. A detailed characterization of inward-facing conformations of the Na+-dependent sugar transporter from Vibrio parahaemolyticus (vSGLT) has previously been reported, but structural details on additional conformations and on how Na+ and ligand influence the equilibrium between other states remains unknown. Here, double electron-electron resonance spectroscopy, structural modeling, and molecular dynamics are utilized to deduce ligand-dependent equilibria shifts of vSGLT in micelles. In the absence and presence of saturating amounts of Na+, vSGLT favors an inward-facing conformation. Upon binding both Na+ and sugar, the equilibrium shifts toward either an outward-facing or occluded conformation. While Na+ alone does not stabilize the outward-facing state, gating charge calculations together with a kinetic model of transport suggest that the resting negative membrane potential of the cell, absent in detergent-solubilized samples, may stabilize vSGLT in an outward-open conformation where it is poised for binding external sugars. In total, these findings provide insights into ligand-induced conformational selection and delineate the transport cycle of vSGLT.

Keywords: DEER; conformation; sugar; transport; vSGLT.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Biological Transport, Active
  • Cysteine / genetics
  • Electron Spin Resonance Spectroscopy / methods
  • Galactose / metabolism
  • Membrane Lipids / chemistry
  • Membrane Lipids / metabolism
  • Micelles
  • Models, Molecular
  • Molecular Dynamics Simulation
  • Mutation
  • Protein Conformation
  • Sodium / metabolism
  • Sodium-Glucose Transport Proteins / chemistry*
  • Sodium-Glucose Transport Proteins / metabolism*
  • Vibrio parahaemolyticus / chemistry

Substances

  • Bacterial Proteins
  • Membrane Lipids
  • Micelles
  • Sodium-Glucose Transport Proteins
  • Sodium
  • Cysteine
  • Galactose