Qu Shaogang, Kanner Baruch I
Department of Biochemistry, Hebrew University Hadassah Medical School, Jerusalem 91120, Israel.
J Biol Chem. 2008 Sep 26;283(39):26391-400. doi: 10.1074/jbc.M802401200. Epub 2008 Jul 25.
To explore rearrangements of the reentrant loop HP2 relative to transmembrane domains (TMs) 7 and 8 during transport by the glial glutamate transporter GLT-1/EAAT2, cysteine pairs were introduced at the extracellular ends of these structural elements. The pairs were introduced around 10-15 A "above" the residues, which make contact with substrate in the related archaeal homologue Glt(Ph). Transport by the double mutants M449C/L466C (HP2/TM 8), L453C/I463C (HP2/TM 8), and I411C/I463C (TM 7/TM 8) was inhibited by copper(II)(1,10-phenanthroline)(3) (CuPh) and by Cd(2+). Inhibition was only observed when the two cysteines were present in the same construct, but not with the respective single cysteine mutants or when only one cysteine was paired with a mutation to another residue. Glutamate and potassium, both expected to increase the proportion of inward-facing transporters, significantly protected against the inhibition of transport activity of M449C/L466C by CuPh. The non-transportable analogues kainate and d, l-threo-beta-benzyloxyaspartate are expected to stabilize an outward-facing conformation, but only the latter potentiated the effect of CuPh on M449C/L466C. However, both analogues increased the aqueous accessibility of the cysteines introduced at positions 449 and 466 to a membrane-impermeant sulfhydryl reagent. Inhibition of L453C/I463C by CuPh was protected not only by glutamate but also by the two analogues. In contrast, these ligands had very little effect on the inhibition of I411C/I463C by CuPh. Our results are consistent with the proposal that HP2 serves as the extracellular gate of the transporter and indicate that glutamate and the two analogues induce distinct conformations of HP2.
为了探究在胶质细胞谷氨酸转运体GLT-1/EAAT2转运过程中,折返环HP2相对于跨膜结构域(TMs)7和8的重排情况,在这些结构元件的胞外端引入了半胱氨酸对。这些半胱氨酸对被引入到比相关古细菌同源物Glt(Ph)中与底物接触的残基“上方”约10 - 15埃处。双突变体M449C/L466C(HP2/TM 8)、L453C/I463C(HP2/TM 8)和I411C/I463C(TM 7/TM 8)的转运受到铜(II)(1,10 - 菲咯啉)(3)(CuPh)和镉(2+)的抑制。仅当两个半胱氨酸存在于同一构建体中时才观察到抑制作用,而在各自的单个半胱氨酸突变体中未观察到抑制作用,或者当只有一个半胱氨酸与另一个残基的突变配对时也未观察到抑制作用。谷氨酸和钾都预期会增加向内构象转运体的比例,它们显著保护M449C/L466C的转运活性免受CuPh的抑制。不可转运类似物红藻氨酸和d,l - 苏式 - β - 苄氧基天冬氨酸预期会稳定向外构象,但只有后者增强了CuPh对M449C/L466C的作用。然而,这两种类似物都增加了在449和466位引入的半胱氨酸对膜不透性巯基试剂的水相可及性。CuPh对L45C/I463C的抑制不仅受到谷氨酸的保护,还受到这两种类似物的保护。相比之下,这些配体对CuPh抑制I411C/I463C的作用影响很小。我们的结果与HP2作为转运体胞外门控的提议一致,并表明谷氨酸和这两种类似物诱导HP2形成不同的构象。