Fulkerson J F, Mobley H L
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
J Bacteriol. 2000 Mar;182(6):1722-30. doi: 10.1128/JB.182.6.1722-1730.2000.
NixA, the high-affinity cytoplasmic membrane nickel transport protein of Helicobacter pylori, imports Ni(2+) into the cell for insertion into the active site of the urease metalloenzyme, which is required for gastric colonization. NixA fractionates with the cytoplasmic membrane, and protein cross-linking studies suggest that NixA functions as a monomer. A preliminary topological model of NixA with seven transmembrane domains was previously proposed based on hydropathy, charge dispersion, and homology to other transporters. To test the proposed topology of NixA and relate critical residues to specific structural elements, a series of 21 NixA-LacZ and 21 NixA-PhoA fusions were created along the entire length of the protein. Expression of reporter fusions was confirmed by Western blotting with beta-galactosidase- and alkaline phosphatase-specific antisera. The activities of reporter fusions near to and upstream of the predicted translational initiation demonstrated the presence of an additional amino-terminal transmembrane domain including a membrane localization signal. Activities of fusions immediately adjacent to motifs which have been shown to be requisite for Ni(2+) transport localized these motifs entirely within transmembrane domains II and III. Fusion activities localized six additional Asp and Glu residues which reduced Ni(2+) transport by >90% when mutated within or immediately adjacent to transmembrane domains II, V, VI, and VII. All fusions strongly support a model of NixA in which the amino and carboxy termini are located in the cytoplasm and the protein possesses eight transmembrane domains.
NixA是幽门螺杆菌的高亲和力细胞质膜镍转运蛋白,它将Ni(2+)导入细胞,以便插入脲酶金属酶的活性位点,这是在胃中定殖所必需的。NixA与细胞质膜分离,蛋白质交联研究表明NixA以单体形式发挥作用。先前基于亲水性、电荷分散以及与其他转运蛋白的同源性,提出了一个具有七个跨膜结构域的NixA初步拓扑模型。为了测试所提出的NixA拓扑结构,并将关键残基与特定结构元件联系起来,沿着蛋白质的全长创建了一系列21个NixA-LacZ和21个NixA-PhoA融合体。通过用β-半乳糖苷酶和碱性磷酸酶特异性抗血清进行蛋白质印迹法,证实了报告基因融合体的表达。预测翻译起始位点附近和上游的报告基因融合体的活性表明存在一个额外的氨基末端跨膜结构域,包括一个膜定位信号。紧邻已被证明是Ni(2+)转运所必需的基序的融合体活性将这些基序完全定位在跨膜结构域II和III内。融合体活性定位了另外六个天冬氨酸和谷氨酸残基,当它们在跨膜结构域II、V、VI和VII内或紧邻其处发生突变时,Ni(2+)转运减少>90%。所有融合体都有力地支持了一个NixA模型,其中氨基和羧基末端位于细胞质中,并且该蛋白质具有八个跨膜结构域。