Nanatani Kei, Maloney Peter C, Abe Keietsu
Department of Molecular and Cell Biology, Tohoku University, Sendai, Japan.
J Bacteriol. 2009 Apr;191(7):2122-32. doi: 10.1128/JB.00830-08. Epub 2009 Jan 30.
AspT, the aspartate:alanine antiporter of Tetragenococcus halophilus, a membrane protein of 543 amino acids with 10 putative transmembrane (TM) helices, is the prototype of the aspartate:alanine exchanger (AAE) family of transporters. Because TM3 (isoleucine 64 to methionine 85) has many amino acid residues that are conserved among members of the AAE family and because TM3 contains two charged residues and four polar residues, it is thought to be located near (or to form part of) the substrate translocation pathway that includes the binding site for the substrates. To elucidate the role of TM3 in the transport process, we carried out cysteine-scanning mutagenesis. The substitutions of tyrosine 75 and serine 84 had the strongest inhibitory effects on transport (initial rates of l-aspartate transport were below 15% of the rate for cysteine-less AspT). Considerable but less-marked effects were observed upon the replacement of methionine 70, phenylalanine 71, glycine 74, arginine 76, serine 83, and methionine 85 (initial rates between 15% and 30% of the rate for cysteine-less AspT). Introduced cysteine residues at the cytoplasmic half of TM3 could be labeled with Oregon green maleimide (OGM), whereas cysteines close to the periplasmic half (residues 64 to 75) were not labeled. These results suggest that TM3 has a hydrophobic core on the periplasmic half and that hydrophilic residues on the cytoplasmic half of TM3 participate in the formation of an aqueous cavity in membranes. Furthermore, the presence of l-aspartate protected the cysteine introduced at glycine 62 against a reaction with OGM. In contrast, l-aspartate stimulated the reactivity of the cysteine introduced at proline 79 with OGM. These results demonstrate that TM3 undergoes l-aspartate-induced conformational alterations. In addition, nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses and a glutaraldehyde cross-linking assay suggest that functional AspT forms homo-oligomers as a functional unit.
丙氨酸反向转运蛋白AspT是一种含有543个氨基酸、具有10个假定跨膜(TM)螺旋的膜蛋白,是天冬氨酸:丙氨酸交换体(AAE)家族转运蛋白的原型。由于TM3(异亮氨酸64至甲硫氨酸85)有许多在AAE家族成员中保守的氨基酸残基,并且由于TM3含有两个带电荷残基和四个极性残基,所以认为它位于包括底物结合位点的底物转运途径附近(或构成其一部分)。为了阐明TM3在转运过程中的作用,我们进行了半胱氨酸扫描诱变。酪氨酸75和丝氨酸84的取代对转运具有最强的抑制作用(L-天冬氨酸转运的初始速率低于无半胱氨酸AspT速率的15%)。当甲硫氨酸70、苯丙氨酸71、甘氨酸74、精氨酸76、丝氨酸83和甲硫氨酸85被取代时,观察到相当但不太明显的影响(初始速率为无半胱氨酸AspT速率的15%至30%)。在TM3胞质半段引入的半胱氨酸残基可用俄勒冈绿马来酰亚胺(OGM)标记,而靠近周质半段的半胱氨酸(残基64至75)未被标记。这些结果表明,TM3在周质半段有一个疏水核心,并且TM3胞质半段的亲水性残基参与膜中水性腔的形成。此外,L-天冬氨酸的存在保护在甘氨酸62处引入的半胱氨酸不与OGM反应。相反,L-天冬氨酸刺激在脯氨酸79处引入的半胱氨酸与OGM的反应性。这些结果表明TM3经历L-天冬氨酸诱导的构象改变。此外,非还原十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析和戊二醛交联试验表明,功能性AspT作为功能单元形成同型寡聚体。