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通过共聚焦显微镜监测泛素包被细菌。

Monitoring Ubiquitin-Coated Bacteria via Confocal Microscopy.

作者信息

Lork Marie, Delvaeye Mieke, Gonçalves Amanda, Van Hamme Evelien, Beyaert Rudi

机构信息

Unit of Molecular Signal Transduction in Inflammation, Inflammation Research Center, VIB, Ghent, Belgium.

Department of Biomedical Molecular Biology, Ghent University, Technologiepark 927, Zwijnaarde, Ghent, 9052, Belgium.

出版信息

Methods Mol Biol. 2016;1449:243-50. doi: 10.1007/978-1-4939-3756-1_14.

Abstract

Salmonella is a gram-negative facultative intracellular pathogen that is capable of infecting a variety of hosts. Inside host cells, most Salmonella bacteria reside and replicate within Salmonella-containing vacuoles. They use virulence proteins to manipulate the host cell machinery for their own benefit and hijack the host cytoskeleton to travel toward the perinuclear area. However, a fraction of bacteria escapes into the cytosol where they get decorated with a dense layer of polyubiquitin, which labels the bacteria for clearance by autophagy. More specifically, autophagy receptor proteins recognize the ubiquitinated bacteria and deliver them to autophagosomes, which subsequently fuse to lysosomes. Here, we describe methods used to infect HeLa cells with Salmonella bacteria and to detect their ubiquitination via immunofluorescence and laser scanning confocal microscopy.

摘要

沙门氏菌是一种革兰氏阴性兼性胞内病原体,能够感染多种宿主。在宿主细胞内,大多数沙门氏菌细菌在含沙门氏菌的液泡中驻留并复制。它们利用毒力蛋白操纵宿主细胞机制以谋取自身利益,并劫持宿主细胞骨架向核周区域移动。然而,一小部分细菌会逃逸到细胞质中,在那里它们会被一层密集的多聚泛素修饰,这会标记这些细菌以便通过自噬清除。更具体地说,自噬受体蛋白识别泛素化的细菌并将它们递送至自噬体,自噬体随后与溶酶体融合。在这里,我们描述了用沙门氏菌感染HeLa细胞并通过免疫荧光和激光扫描共聚焦显微镜检测其泛素化的方法。

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