Journal Article FZJ-2020-03832

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Na + -dependent gate dynamics and electrostatic attraction ensure substrate coupling in glutamate transporters

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2020
Assoc. Washington, DC [u.a.]

Science advances 6(47), eaba9854 - () [10.1126/sciadv.aba9854]

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Abstract: Excitatory amino acid transporters (EAATs) harness [Na+], [K+], and [H+] gradients for fast and efficient glutamate removal from the synaptic cleft. Since each glutamate is cotransported with three Na+ ions, [Na+] gradients are the predominant driving force for glutamate uptake. We combined all-atom molecular dynamics simulations, fluorescence spectroscopy, and x-ray crystallography to study Na+:substrate coupling in the EAAT homolog GltPh. A lipidic cubic phase x-ray crystal structure of wild-type, Na+-only bound GltPh at 2.5-Å resolution revealed the fully open, outward-facing state primed for subsequent substrate binding. Simulations and kinetic experiments established that only the binding of two Na+ ions to the Na1 and Na3 sites ensures complete HP2 gate opening via a conformational selection-like mechanism and enables high-affinity substrate binding via electrostatic attraction. The combination of Na+-stabilized gate opening and electrostatic coupling of aspartate to Na+ binding provides a constant Na+:substrate transport stoichiometry over a broad range of neurotransmitter concentrations.

Classification:

Contributing Institute(s):
  1. Molekular- und Zellphysiologie (IBI-1)
  2. Strukturbiochemie (IBI-7)
  3. JARA - HPC (JARA-HPC)
Research Program(s):
  1. 551 - Functional Macromolecules and Complexes (POF3-551) (POF3-551)
  2. MOLECULAR MODELLING OF BIFUNCTIONAL MEMBRANE TRANSPORT PROTEINS (jics40_20190501) (jics40_20190501)
  3. Molecular dynamics simulations of P2X receptors (jara0180_20200501) (jara0180_20200501)
  4. Multiscale simulations of voltage-gated sodium channel complexes and clusters (jics42_20191101) (jics42_20191101)
  5. Molecular dynamics of the SLC26 family of ion channels and transporters (jara0177_20191101) (jara0177_20191101)

Appears in the scientific report 2020
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Dokumenttypen > Aufsätze > Zeitschriftenaufsätze
JARA > JARA > JARA-JARA\-HPC
Institutssammlungen > IBI > IBI-7
Institutssammlungen > IBI > IBI-1
Workflowsammlungen > Öffentliche Einträge
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