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无细胞细菌分裂原环的生物发生,该原环可以收缩脂质体。

Cell-free biogenesis of bacterial division proto-rings that can constrict liposomes.

机构信息

Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, van der Maasweg 9, 2629HZ, Delft, The Netherlands.

Centro de Investigaciones Biológicas Margarita Salas, CSIC, 28040, Madrid, Spain.

出版信息

Commun Biol. 2020 Sep 30;3(1):539. doi: 10.1038/s42003-020-01258-9.

Abstract

A major challenge towards the realization of an autonomous synthetic cell resides in the encoding of a division machinery in a genetic programme. In the bacterial cell cycle, the assembly of cytoskeletal proteins into a ring defines the division site. At the onset of the formation of the Escherichia coli divisome, a proto-ring consisting of FtsZ and its membrane-recruiting proteins takes place. Here, we show that FtsA-FtsZ ring-like structures driven by cell-free gene expression can be reconstituted on planar membranes and inside liposome compartments. Such cytoskeletal structures are found to constrict the liposome, generating elongated membrane necks and budding vesicles. Additional expression of the FtsZ cross-linker protein ZapA yields more rigid FtsZ bundles that attach to the membrane but fail to produce budding spots or necks in liposomes. These results demonstrate that gene-directed protein synthesis and assembly of membrane-constricting FtsZ-rings can be combined in a liposome-based artificial cell.

摘要

实现自主合成细胞的主要挑战在于将分裂机制编码到遗传程序中。在细菌细胞周期中,细胞骨架蛋白组装成环来定义分裂位点。在大肠杆菌分裂体形成的开始时,由 FtsZ 及其膜招募蛋白组成的原环开始形成。在这里,我们表明可以在平面膜和脂质体隔室内部重新构建由无细胞基因表达驱动的 FtsA-FtsZ 环样结构。这些细胞骨架结构被发现可收缩脂质体,产生伸长的膜颈和出芽小泡。额外表达 FtsZ 交联蛋白 ZapA 会产生更刚性的 FtsZ 束,这些束附着在膜上,但不能在脂质体中产生出芽斑点或颈部。这些结果表明,基于基因的蛋白质合成和膜收缩 FtsZ 环的组装可以在基于脂质体的人工细胞中结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d71/7527988/95bb9c9a6d93/42003_2020_1258_Fig1_HTML.jpg

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