Kim Sanguk, Chamberlain Aaron K, Bowie James U
Department of Chemistry and Biochemistry, University of California Los Angeles-Department of Energy Center for Genomics and Proteomics, Molecular Biology Institute, Boyer Hall, University of California, Los Angeles, CA 90095-1570, USA.
Proc Natl Acad Sci U S A. 2004 Apr 20;101(16):5988-91. doi: 10.1073/pnas.0308694101. Epub 2004 Apr 5.
Helicobacter pylori is a human pathogen responsible for severe gastric diseases such as peptic ulcers, gastric adenocarcinoma, and gastric lymphoma. Vacuolating toxin (VacA) is crucial in facilitating the colonization of the gastric lining by inducing cell apoptosis and immune suppression. VacA inserts into membranes and forms a hexameric, anion-selective pore. Here we present a structural model of the VacA pore that strongly resembles the structure of an unrelated anion-selective channel, MscS. In our model, Gly residues in GXXXG motifs pack against small Ala or Val side chains to generate the pore. Our model suggests that the same design of two anion-selective channels was achieved by two different evolutionary paths and provides insight into the mechanism of VacA function.
幽门螺杆菌是一种人类病原体,可引发严重的胃部疾病,如消化性溃疡、胃腺癌和胃淋巴瘤。空泡毒素(VacA)通过诱导细胞凋亡和免疫抑制,在促进胃黏膜定植方面起着关键作用。VacA插入细胞膜并形成六聚体的阴离子选择性孔道。在此,我们展示了VacA孔道的结构模型,该模型与一种无关的阴离子选择性通道MscS的结构极为相似。在我们的模型中,GXXXG基序中的甘氨酸残基与小的丙氨酸或缬氨酸侧链堆积,从而形成孔道。我们的模型表明,两种阴离子选择性通道通过两条不同的进化路径实现了相同的设计,并为VacA功能机制提供了见解。