Department of Medical Biotechnology, Institute of Health Sciences, Acibadem University, Atasehir, Istanbul, Turkey.
Department of Biostatistics and Medical Informatics, School of Medicine, Acibadem University, Atasehir, Istanbul, Turkey.
PLoS One. 2024 Oct 29;19(10):e0300557. doi: 10.1371/journal.pone.0300557. eCollection 2024.
Outer membrane proteins (OMPs) play a key role in facilitating the survival of Helicobacter pylori within the gastric tissue by mediating adherence. Among these proteins, Outer inflammatory protein A (OipA) is a critical factor in H. pylori colonization of the host gastric epithelial cell surface. While the role of OipA in H. pylori attachment and its association with clinical outcomes have been established, the structural mechanisms underlying OipA's action in adherence to gastric epithelial cells remain limited. Our study employed experimental and computational approaches to investigate the interaction partners of OipA on the gastric epithelial cell surface. Initially, we conducted a proteomic analysis using a pull-down assay with recombinant OipA and gastric epithelial cell membrane proteins to identify the OipA interactome. This analysis revealed 704 unique proteins that interacted with OipA. We subsequently analyzed 16 of these OipA partners using molecular modeling tools. Among these 16 partners, we highlight three human proteins, namely Hepatocyte growth factor (HGF), Mesenchymal epithelial transition factor receptor (Met), and Adhesion G Protein-Coupled Receptor B1 (AGRB1) that could play a role in H. pylori adherence to the gastric epithelial cell surface with OipA. Collectively, these findings reveal novel host interactions mediated by OipA, suggesting their potential as therapeutic targets for combating H. pylori infection.
外膜蛋白(OMPs)在介导黏附中发挥关键作用,促进幽门螺杆菌在胃组织中的存活。在这些蛋白中,外炎性蛋白 A(OipA)是幽门螺杆菌定植宿主胃上皮细胞表面的关键因素。虽然 OipA 在幽门螺杆菌附着中的作用及其与临床结果的关联已经确定,但 OipA 在上皮细胞附着中作用的结构机制仍有限。我们的研究采用实验和计算方法研究了 OipA 在胃上皮细胞表面的相互作用伙伴。最初,我们使用重组 OipA 和胃上皮细胞膜蛋白进行下拉测定进行蛋白质组学分析,以鉴定 OipA 的相互作用组。该分析揭示了与 OipA 相互作用的 704 种独特蛋白质。随后,我们使用分子建模工具分析了其中的 16 个 OipA 伙伴。在这 16 个伙伴中,我们重点介绍了三种人类蛋白,即肝细胞生长因子(HGF)、间质上皮转化因子受体(Met)和粘附 G 蛋白偶联受体 B1(AGRB1),它们可能与 OipA 一起参与幽门螺杆菌附着到胃上皮细胞表面。总之,这些发现揭示了 OipA 介导的新的宿主相互作用,表明它们有潜力成为对抗幽门螺杆菌感染的治疗靶点。