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收缩性注射系统的原位结构、功能及进化

In situ architecture, function, and evolution of a contractile injection system.

作者信息

Böck Désirée, Medeiros João M, Tsao Han-Fei, Penz Thomas, Weiss Gregor L, Aistleitner Karin, Horn Matthias, Pilhofer Martin

机构信息

Institute of Molecular Biology and Biophysics, Eidgenössische Technische Hochschule Zürich, CH-8093 Zürich, Switzerland.

Division of Microbial Ecology, University of Vienna, A-1090 Vienna, Austria.

出版信息

Science. 2017 Aug 18;357(6352):713-717. doi: 10.1126/science.aan7904.

Abstract

Contractile injection systems mediate bacterial cell-cell interactions by a bacteriophage tail-like structure. In contrast to extracellular systems, the type 6 secretion system (T6SS) is defined by intracellular localization and attachment to the cytoplasmic membrane. Here we used cryo-focused ion beam milling, electron cryotomography, and functional assays to study a T6SS in The in situ architecture revealed three modules, including a contractile sheath-tube, a baseplate, and an anchor. All modules showed conformational changes upon firing. Lateral baseplate interactions coordinated T6SSs in hexagonal arrays. The system mediated interactions with host membranes and may participate in phagosome escape. Evolutionary sequence analyses predicted that T6SSs are more widespread than previously thought. Our insights form the basis for understanding T6SS key concepts and exploring T6SS diversity.

摘要

收缩注射系统通过噬菌体尾部样结构介导细菌细胞间相互作用。与细胞外系统不同,6型分泌系统(T6SS)的定义是其定位于细胞内并附着于细胞质膜。在此,我们使用低温聚焦离子束铣削、电子冷冻断层扫描和功能测定法来研究一种T6SS。原位结构揭示了三个模块,包括收缩鞘管、基板和锚定物。所有模块在激发时均显示构象变化。基板横向相互作用协调了六边形阵列中的T6SS。该系统介导与宿主膜的相互作用,并可能参与吞噬体逃逸。进化序列分析预测T6SS比以前认为的更为广泛。我们的见解为理解T6SS关键概念和探索T6SS多样性奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9770/6485382/9d38a8c86b30/emss-78854-f001.jpg

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