通过负染色电子断层扫描分析支原体移动滑行机械的内部结构。

IF 1.6 Q4 BIOPHYSICS Biophysics and physicobiology Pub Date : 2024-05-28 eCollection Date: 2024-01-01 DOI:10.2142/biophysico.bppb-v21.0015
Minoru Fukushima, Takuma Toyonaga, Yuhei O Tahara, Daisuke Nakane, Makoto Miyata
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引用次数: 0

摘要

移动支原体是一种寄生细菌,它在细胞极上形成滑行机制,并沿着细胞极的方向在固体表面滑行。滑行机械由内部结构和表面结构组成。内部结构分为位于前端的钟状结构和从钟状结构延伸出来的链状结构。本研究利用负染色电子显微镜和电子断层扫描分析了在不同条件下制备的内部结构。链状结构是由包含两个类似于 ATP 合成酶的复合物的链接马达构成的。马达之间有一个最大直径为 6 纳米、高 13 纳米的圆柱形间隔物,以及直径为 0.9-8.3 纳米、长度为 14.7±6.9 纳米的匿名连接体。喇叭口呈碗状,表面呈蜂窝状,周期为 8.4 nm。电机链通过一个楔形结构与钟罩边缘连接。这些结构可能在滑翔机械单元的组装和合作中发挥作用。
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Internal structure of Mycoplasma mobile gliding machinery analyzed by negative staining electron tomography.

Mycoplasma mobile is a parasitic bacterium that forms gliding machinery on the cell pole and glides on a solid surface in the direction of the cell pole. The gliding machinery consists of both internal and surface structures. The internal structure is divided into a bell at the front and chain structure extending from the bell. In this study, the internal structures prepared under several conditions were analyzed using negative-staining electron microscopy and electron tomography. The chains were constructed by linked motors containing two complexes similar to ATP synthase. A cylindrical spacer with a maximum diameter of 6 nm and a height of 13 nm, and anonymous linkers with a diameter of 0.9-8.3 nm and length of 14.7±6.9 nm were found between motors. The bell is bowl-shaped and features a honeycomb surface with a periodicity of 8.4 nm. The chains of the motor are connected to the rim of the bell through a wedge-shaped structure. These structures may play roles in the assembly and cooperation of gliding machinery units.

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Chemical tongues as multipurpose bioanalytical tools for the characterization of complex biological samples. Unraveling the fastest myosin: Discovery history and structure-function relationships of algae Chara myosin XI. Internal structure of Mycoplasma mobile gliding machinery analyzed by negative staining electron tomography. Application of single-molecule analysis to singularity phenomenon of cells. X-ray diffraction recording from a small amount of fibrous protein materials oriented by a micro shear-flow cell.
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