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Neurotransmitter sodium symporter

(Redirected from Sodium:neurotransmitter symporter)

A neurotransmitter sodium symporter (NSS) (TC# 2.A.22) is type of neurotransmitter transporter that catalyzes the uptake of a variety of neurotransmitters, amino acids, osmolytes and related nitrogenous substances by a solute:Na+ symport mechanism.[1][2] The NSS family is a member of the APC superfamily. Its constituents have been found in bacteria, archaea and eukaryotes.

Sodium:neurotransmitter symporter family
Identifiers
SymbolSNF
PfamPF00209
InterProIPR000175
PROSITEPDOC00533
SCOP22a65 / SCOPe / SUPFAM
TCDB2.A.22
OPM superfamily64
OPM protein2a65
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Function

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Neurotransmitter transport systems are responsible for the release, re-uptake and recycling of neurotransmitters at synapses. High affinity transport proteins found in the plasma membrane of presynaptic nerve terminals and glial cells are responsible for the removal, from the extracellular space, of released-transmitters, thereby terminating their actions.[3]

The majority of the transporters constitute an extensive family of homologous proteins that derive energy from the co-transport of Na+ and Cl−, in order to transport neurotransmitter molecules into the cell against their concentration gradient.

Neurotransmitter sodium symporters (NSS) are targets for anti-depressants, psychostimulants and other drugs.[4]

Transport reaction

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The generalized transport reaction for the members of this family is:[2]

solute (out) + Na+ (out) → solute (in) + Na+ (in).

Structure

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The family has a common structure of 12 presumed transmembrane helices and includes carriers for gamma-aminobutyric acid (GABA), noradrenaline/adrenaline, dopamine, serotonin, proline, glycine, choline, betaine, taurine and other small molecules.[2]

NSS carriers are structurally distinct from the second more-restricted family of plasma membrane transporters, which are responsible for excitatory amino acid transport (see TC# 2.A.23). The latter couple glutamate and aspartate uptake to the cotransport of Na+ and the counter-transport of K+, with no apparent dependence on Cl−.[5] In addition, both of these transporter families are distinct from the vesicular neurotransmitter transporters.[6][7] Sequence analysis of the Na+/Cl− neurotransmitter superfamily reveals that it can be divided into four subfamilies, these being transporters for monoamines, the amino acids proline and glycine, GABA, and a group of orphan transporters.[8]

Tavoulari et al. (2011) described conversion of the Cl− -independent prokaryotic tryptophan transporter TnaT (2.A.22.4.1) to a fully functional Cl− -dependent form by a single point mutation, D268S. Mutations in TnaT-D268S, in wild type TnaT and in a serotonin transporter (SERT; 2.A.22.1.1) provided direct evidence for the involvement of each of the proposed residues in Cl− coordination. In both SERT and TnaT-D268S, Cl− and Na+ mutually increase each other's potency, consistent with electrostatic interaction through adjacent binding sites.[9]

Crystal structures

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There are several crystal structures available for a couple members of the NSS family:

Subfamilies

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Several characterized proteins are classified within the NSS family and can be found in the Transporter Classification Database.

Human proteins containing this domain

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SLC6A1, SLC6A2, SLC6A3, SLC6A4, SLC6A5, SLC6A6, SLC6A7, SLC6A8, SLC6A9, SLC6A11, SLC6A12, SLC6A13, SLC6A14, SLC6A15, SLC6A16, SLC6A17, SLC6A18, SLC6A19, SLC6A20

See also

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References

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  1. ^ Rudnick, G; Krämer, R; Blakely, RD; Murphy, DL; Verrey, F (January 2014). "The SLC6 transporters: perspectives on structure, functions, regulation, and models for transporter dysfunction" (PDF). Pflügers Archiv. 466 (1): 25–42. doi:10.1007/s00424-013-1410-1. PMC 3930102. PMID 24337881.
  2. ^ a b c Saier, MH Jr. "2.A.22 The Neurotransmitter:Sodium Symporter (NSS) Family". Transporter Classification Database.
  3. ^ Attwell D, Bouvier M (1992). "Cloners quick on the uptake". Curr. Biol. 2 (10): 541–543. Bibcode:1992CBio....2..541A. doi:10.1016/0960-9822(92)90024-5. PMID 15336049. S2CID 2334406.
  4. ^ Zomot, E; Bendahan, A; Quick, M; Zhao, Y; Javitch, JA; Kanner, BI (October 11, 2007). "Mechanism of chloride interaction with neurotransmitter:sodium symporters". Nature. 449 (7163): 726–30. Bibcode:2007Natur.449..726Z. doi:10.1038/nature06133. PMID 17704762. S2CID 4391735.
  5. ^ Malandro MS, Kilberg MS (1996). "Molecular biology of mammalian amino acid transporters". Annu. Rev. Biochem. 65: 305–336. doi:10.1146/annurev.bi.65.070196.001513. PMID 8811182.
  6. ^ Arriza JL, Amara SG (1993). "Neurotransmitter transporters: three distinct gene families". Curr. Opin. Neurobiol. 3 (3): 337–344. doi:10.1016/0959-4388(93)90126-J. PMID 8103691. S2CID 41721766.
  7. ^ Uhl GR, Johnson PS (1994). "Neurotransmitter transporters: three important gene families for neuronal function". J. Exp. Biol. 196: 229–236. doi:10.1242/jeb.196.1.229. PMID 7823024.
  8. ^ Nelson N, Lill H (1998). "Homologies and family relationships among Na+/Cl− neurotransmitter transporters". Neurotransmitter Transporters. Methods in Enzymology. Vol. 296. pp. 425–436. doi:10.1016/S0076-6879(98)96030-X. ISBN 978-0-12-182197-5. PMID 9779464.
  9. ^ Tavoulari, S; Rizwan, AN; Forrest, LR; Rudnick, G (January 28, 2011). "Reconstructing a chloride-binding site in a bacterial neurotransmitter transporter homologue". Journal of Biological Chemistry. 286 (4): 2834–42. doi:10.1074/jbc.M110.186064. PMC 3024779. PMID 21115480.
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