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Observation of the intracellular behavior of recombinant Yersinia pseudotuberculosis invasin protein.

机译:重组耶尔森氏菌假结核侵袭素蛋白的细胞内行为观察。

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In this study, we observed the intracellular behavior of recombinant invasin, a 103-kDa outer membrane protein of Yersinia pseudotuberculosis. To mimic the in vivo behavior of bacterial invasin, a polyvalent form of invasin was generated by incubation of biotinylated GST-fused invasin C-terminal portion protein (GST-INVS) with avidin. Several experiments confirmed that the recombinant invasin could consistently reproduce the invasin-mediated entry to mammalian epithelial cells. We analyzed the molecular kinetics of polyvalent INVS by western blotting, (125) I-uptake, and immunofluorescent microscopy. The internalized polyvalent INVS was rapidly translocated to the RIPA-insoluble (polymerized-actin enriched) fraction and formed cytoplasmic vesicles, while monovalent invasin did not show such kinetics. From these observations, we concluded that our bacterial-free system is able to analyze the action of invasin for Yersinia pseudotuberculosis entry.
机译:在这项研究中,我们观察到了重组拟南芥(Invasin)的细胞内行为,后者是一种假性耶尔森菌(Yersinia pseudotuberculosis)的103 kDa外膜蛋白。为了模拟细菌侵袭素的体内行为,通过将生物素化的GST融合的侵袭素C端部分蛋白(GST-INVS)与亲和素一起孵育来生成侵袭素的多价形式。几项实验证实,重组侵入蛋白可以一致地复制侵入蛋白介导的进入哺乳动物上皮细胞。我们通过蛋白质印迹,(125)I摄取和免疫荧光显微镜分析了多价INVS的分子动力学。内部化的多价INVS迅速转移到RIPA不溶(富集聚合肌动蛋白的部分)并形成细胞质囊泡,而单价入侵素则没有这种动力学。从这些观察结果,我们得出结论,我们的无细菌系统能够分析浸润素对假性耶尔森氏菌进入的作用。

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