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Structure and Function of Neurotransmitter Transporters Erice 2011
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Sodium-Coupled Neurotransmitter Transporters Role of neurotransmitter transporters (NSS and glutamate). Electrophysiology as a tool to analyze transporter function. NSS transporters: structure, function and chloride site. Glutamate transporters are different.
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Forrest, L.R. and Rudnick, G.(2009 Physiology 24, 377-386
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Role of neurotransmitter transporters
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Giros et.al. (1996) Nature 397, 606-612
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Electrophysiology as a tool to analyze Transporter Function Most neurotransmitter transporters are electrogenic cotransporters using multiple sodium ions as well as chloride (NSS) or potassium (glutamate transporters)
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Resistive currents: Electrogenic transport current voltage time
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Example of a common experimental protocol -25 Current (nA) Voltage (mV) -150 + 50 time 0 Protocol of Voltage jumps: the holding voltage is -25 mV 8 voltage jumps with 25 mV intervals Substrate-induced inward currents
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Capacitative currents: a consequence of Sodium binding/unbinding current voltage time
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NSS transporters: structure, function and chloride site. Eukaryotic NSS transporters mediate cotransport of the neurotransmitter sodium and chloride. For istance the GABA transporter GAT-1: 2Na+out +1Cl-out + GABAout → 2Na+in +1Cl-in + GABAin
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NH2 R69 G63 Y140 COOH 2Na + :Cl - :GABA GABA Transporter GAT-1
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Yamashita et. al. (2005) Nature 437, 215-223
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Lithium Interactions In GAT-1, Asp-395 participates in the Na2 site
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Loss of Lithium stimulation in D395 mutants
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Li stimulation in WT depends on [GABA]
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A. GABAB. Lithium D395 mutants have lost the Li leak currents
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Where is the chloride binding site ?
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Rationale Coordination of Cl - in ClC Channels/antiporters by main chain NH and side chain hydroxyls from serine and tyrosine residues Look for serine, threonine and tyrosine residues, located in the transmembrane domains conserved in the Cl - dependent neurotransmitter transporters, but not necessarily in their Cl - independent bacterial counterparts
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Chloride Dependent Chloride Independent Amino acid sequence alignment of a segment of TM VII Between eukaryotic and prokaryotic members of the NSS family
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Only replacements with acidic amino acids render uptake chloride independent uptake in absence / uptake in presence of Chloride in WT and S331 mutants
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WTS331E substrate uptake is Chloride-dependent substrate uptake is Chloride-Independent return of unloaded T accelerated by protonation Transport cycle in WT and S331E
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Uptake of [ 3 H]GABA into reconstituted liposomes inlaid with WT or S331E transporters No uptake in the absence of chloride1)Uptake becomes independent on chloride 2) Lowering internal pH dramatically increases uptake
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Symmetry in NSS transporters A clue to understanding alternating access
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Forrest et.al.(2008) PNAS 105, 10338-10343
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Transmembrane domain 8 of the {gamma}-aminobutyric acid transporter GAT-1 lines a cytoplasmic accessibility pathway into its binding pocket. Ben-Yona A, Kanner BI. J Biol Chem. 2009 Apr 10;284(15):9727-32. Epub 2009 Feb 6
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Controversy on Substrate Binding Stoichiometry in LeuT The mechanism of a neurotransmitter:sodium symporter--inward release of Na+ and Substrate is triggered by substrate in a second binding site. Shi L, Quick M, Zhao Y, Weinstein H, Javitch JA. Mol Cell. 2008 Jun 20;30(6):667-77. Neurotransmitter/sodium symporter orthologue LeuT has a single high-affinity substrate site. Piscitelli CL, Krishnamurthy H, Gouaux E. Nature. 2010 Dec 23;468(7327):1129-32
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Glutamate Transporters are different
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Glutamate transport and currents Cl -
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3Na +,H + T K+K+ K+K+ T T T K+K+ K+K+ AAA - TT nNa +,H + T Na + n,H + AAA - -X AAA - Na + 3,H + AAA - Na + 3,H +
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Control of inside Form liposomes in: KPiNa,glu KPi Na,glu NaCl + glu* NaCl + glu* Net fluxExchange
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Glutamate transporters GltPh: an archeal homologue of brain glutamate transporters Yernool et. al. (2004) Nature 431, 811-818 The structure is in excellent agreement with functional data on site-directed mutants from the mammalian glutamate transporters, including the inferred proximity of the tips of HP1 and HP2.
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Two Tl + binding sites in Glt Ph Boudker et. al. (2007) Nature 445, 387-393
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The side-chain of a conserved aspartate participates in Tl + site 1 Does this aspartate participate in a cation binding site in the brain glutamate transporters?
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3Na +,H + T K+K+ K+K+ T T T K+K+ K+K+ AAA - TT nNa +,H + T Na + n,H + AAA - -X AAA - Na + 3,H + AAA - Na + 3,H +
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D-[ 3 H]-AspL-[ 3 H]-Asp L-[ 3 H]-Glu
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3Na +,H + T K+K+ K+K+ T T T K+K+ K+K+ AAA - TT nNa +,H + T Na + n,H + AAA - -X AAA - Na + 3,H + AAA - Na + 3,H +
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N Reyes et al. Nature 000, 1-6 (2009) doi:10.1038/nature08616 Schematic transport mechanism.
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GAT-1 and other NSS Hebrew Univ. Columbia Univ. Annie Bendahan Matthias Quick Elia Zomot Yongfang Zhao Assaf Ben-Yona Jonathan Javitch Glutamate Transporters Hebrew Univ MPI Frankfurt Shlomit Teichman Lucy Forrest Shaogang Qu Thomas Crisman Noa Rosental
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