Elucidating Conformational Changes in the {gamma}-Aminobutyric Acid Transporter-1

Anne-Kristine Meinild, Donald D F Loo, Søren Skovstrup Hansen, Ulrik Gether, Nanna Macaulay

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19 Citations (Scopus)

Abstract

The GABA transporter-1 (GAT-1) has three current-generating modes: GABA-coupled current, Li(+)-induced leak current, and Na(+)-dependent transient currents. We earlier hypothesized that Li(+) is able to substitute for the first Na(+) in the transport cycle and thereby induce a distinct conformation in GAT-1 and that the onset of the Li(+)-induced leak current at membrane potentials more negative than -50 mV was due to a voltage-dependent conformational change of the Li(+)-bound transporter. In this study, we set out to verify this hypothesis and seek insight into the structural dynamics underlying the leak current, as well as the sodium-dependent transient currents, by applying voltage clamp fluorometry to tetramethylrhodamine 6-maleimide-labeled GAT-1 expressed in Xenopus laevis oocytes. MTSET accessibility studies demonstrated the presence of two distinct conformations of GAT-1 in the presence of Na(+) or Li(+). The voltage-dependent fluorescence intensity changes obtained in Li(+) buffer correlated with the Li(+)-induced leak currents, i.e. both were highly voltage-dependent and only present at hyperpolarized potentials (<-50 mV). The transient currents correlated directly with the voltage-dependent fluorescence data obtained in sodium buffer and the associated conformational changes were distinct from those associated with the Li(+)-induced leak current. The inhibitor potency of SKF89976A of the Li(+)- versus Na(+)-bound transporter confirmed the cationic dependence of the conformational occupancy. Our observations suggest that the microdomain situated at the external end of transmembrane I is involved in different conformational changes taking place either during the binding and release of sodium or during the initiation of the Li(+)-induced leak current.
Original languageEnglish
JournalJournal of Biological Chemistry
Volume284
Issue number24
Pages (from-to)16226-35
Number of pages9
ISSN0021-9258
DOIs
Publication statusPublished - 2009

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