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Use of Real-Time, Label-Free Analysis in Revealing Low-Affinity Binding to Blood Group Antigens by Helicobacter pylori

机译:实时,无标签分析在揭示幽门螺杆菌与血型抗原的低亲和力结合中的应用

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Infectious diseases are often initiated by microbial adherence that is mediated by the binding of attachment molecules, termed adhesins, to cell surface receptors on host cells. We present an experimental system, oblique-incidence reflectivity difference (OI-RD) microscopy, which allows the detection of novel, low-affinity microbial attachment mechanisms that may be essential for infectious processes. OI-RD microscopy was used to analyze direct binding of the oncopathogen, Helicobacter pylori (H. pylori) to immobilized glycoconjugates in real time with no need for labeling tags. The results suggest the presence of additional Lewis b blood group antigen (Le~(b)) binding adhesins that have not been detected previously. OI-RD microscopy also confirmed the high-affinity binding of H. pylori outer-membrane protein BabA to Le~(b). The OI-RD microscopy method is broadly applicable to real-time characterization of intact microbial binding to host receptors and offers new strategies to elucidate the molecular interactions of infectious agents with human host cells.
机译:感染性疾病通常是由微生物粘附引起的,微生物粘附是由附着分子(称为粘附素)与宿主细胞上细胞表面受体的结合介导的。我们提出了一个实验系统,斜入射反射率差(OI-RD)显微镜,它可以检测可能对感染过程至关重要的新型,低亲和力的微生物附着机制。 OI-RD显微镜用于实时分析致癌菌幽门螺杆菌(H. pylori)与固定的糖结合物的直接结合,而无需标记标签。结果表明存在额外的Lewis b血型抗原(Le〜(b))结合粘附素,而以前尚未检测到。 OI-RD显微镜也证实了幽门螺杆菌的外膜蛋白BabA与Le〜(b)的高亲和力结合。 OI-RD显微镜方法广泛适用于完整微生物与宿主受体结合的实时表征,并为阐明传染原与人类宿主细胞的分子相互作用提供了新的策略。

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