Identification of a 3(rd) Na(+) Binding Site of the Glycine Transporter, GlyT2

The Na(+)/Cl(-) dependent glycine transporters GlyT1 and GlyT2 regulate synaptic glycine concentrations. Glycine transport by GlyT2 is coupled to the co-transport of three Na(+) ions, whereas transport by GlyT1 is coupled to the co-transport of only two Na(+) ions. These differences in ion-flux coupling determine their respective concentrating capacities and have a direct bearing on their functional roles in synaptic transmission. The crystal structures of the closely related bacterial Na(+)-dependent leucine transporter, LeuT(Aa), and the Drosophila dopamine transporter, dDAT, have allowed prediction of two Na(+) binding sites in GlyT2, but the physical location of the third Na(+) site in GlyT2 is unknown. A bacterial betaine transporter, BetP, has also been crystallized and shows structural similarity to LeuT(Aa). Although betaine transport by BetP is coupled to the co-transport of two Na(+) ions, the first Na(+) site is not conserved between BetP and LeuT(Aa), the so called Na1' site. We hypothesized that the third Na(+) binding site (Na3 site) of GlyT2 corresponds to the BetP Na1' binding site. To identify the Na3 binding site of GlyT2, we performed molecular dynamics (MD) simulations. Surprisingly, a Na(+) placed at the location consistent with the Na1' site of BetP spontaneously dissociated from its initial location and bound instead to a novel Na3 site. Using a combination of MD simulations of a comparative model of GlyT2 together with an analysis of the functional properties of wild type and mutant GlyTs we have identified an electrostatically favorable novel third Na(+) binding site in GlyT2 formed by Trp263 and Met276 in TM3, Ala481 in TM6 and Glu648 in TM10.