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TitleCryo-EM structures of excitatory amino acid transporter 3 visualize coupled substrate, sodium, and proton binding and transport.
Journal, issue, pagesSci Adv, Vol. 7, Issue 10, Year 2021
Publish dateMar 3, 2021
AuthorsBiao Qiu / Doreen Matthies / Eva Fortea / Zhiheng Yu / Olga Boudker /
PubMed AbstractHuman excitatory amino acid transporter 3 (hEAAT3) mediates glutamate uptake in neurons, intestine, and kidney. Here, we report cryo-EM structures of hEAAT3 in several functional states where the ...Human excitatory amino acid transporter 3 (hEAAT3) mediates glutamate uptake in neurons, intestine, and kidney. Here, we report cryo-EM structures of hEAAT3 in several functional states where the transporter is empty, bound to coupled sodium ions only, or fully loaded with three sodium ions, a proton, and the substrate aspartate. The structures suggest that hEAAT3 operates by an elevator mechanism involving three functionally independent subunits. When the substrate-binding site is near the cytoplasm, it has a remarkably low affinity for the substrate, perhaps facilitating its release and allowing the rapid transport turnover. The mechanism of the coupled uptake of the sodium ions and the substrate is conserved across evolutionarily distant families and is augmented by coupling to protons in EAATs. The structures further suggest a mechanism by which a conserved glutamate residue mediates proton symport.
External linksSci Adv / PubMed:33658209 / PubMed Central
MethodsEM (single particle)
Resolution2.85 - 3.71 Å
Structure data

EMDB-22011, PDB-6x2l:
hEAAT3-IFS-Na
Method: EM (single particle) / Resolution: 2.85 Å

EMDB-22014, PDB-6x2z:
hEAAT3-OFS-Asp
Method: EM (single particle) / Resolution: 3.03 Å

EMDB-22020, PDB-6x3e:
hEAAT3-Asymmetric-1o2i
Method: EM (single particle) / Resolution: 3.42 Å

EMDB-22021, PDB-6x3f:
hEAAT3-IFS-Apo
Method: EM (single particle) / Resolution: 3.03 Å

EMDB-22022:
hEAAT3-IFS-in10mMGlu
Method: EM (single particle) / Resolution: 2.96 Å

EMDB-22023:
hEAAT3-IFS-in250mM-KCl
Method: EM (single particle) / Resolution: 2.85 Å

EMDB-22024:
hEAAT3-Asymmetric-2o1i-in20mM-Asp
Method: EM (single particle) / Resolution: 3.71 Å

Chemicals

ChemComp-ASP:
ASPARTIC ACID

ChemComp-NA:
Unknown entry

ChemComp-CHT:
CHOLINE ION

Source
  • homo sapiens (human)
KeywordsTRANSPORT PROTEIN / humant Excitatory amino acid transporter 3 / hEAAT3 outward-facing / full-bound / Asymmetric / Outward-facing bound / Inward-facing open / hEAAT3 inward-facing Apo state

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