低温电子断层扫描检测肌动蛋白短丝的几何约束。

Mikhail Kudryashev, Simone Lepper, Wolfgang Baumeister, Marek Cyrklaff, Friedrich Frischknecht
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引用次数: 40

摘要

肌动蛋白聚合成细丝可以推动膜形成延伸,如丝状足或片状足,这在细胞运动和吞噬等过程中是重要的。同样,小的细胞器或病原体也可以通过肌动蛋白聚合来移动。这种肌动蛋白细丝可以排列成不同的图案,并且通过各种电子显微镜方法显示,其长度通常为数百纳米。更短的肌动蛋白丝参与顶复合体寄生虫的运动。然而,这些短丝迄今尚未在完整细胞中可见。在这里,我们使用低温电子断层扫描研究了疟原虫孢子,一种由蚊子传播的疟疾寄生虫的运动形式。我们检测到质膜的丝状延伸,并在质膜下的肺泡上间隙观察到丝状结构。然而,这些丝不能明确地指定为肌动蛋白丝。EM数据收集和层析重建的计算机模拟确定了由于其长度,浓度和方向而导致的细丝暴露的限制。PACS代码:87.64.Ee。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Geometric constrains for detecting short actin filaments by cryogenic electron tomography.

Geometric constrains for detecting short actin filaments by cryogenic electron tomography.

Geometric constrains for detecting short actin filaments by cryogenic electron tomography.

Geometric constrains for detecting short actin filaments by cryogenic electron tomography.

Polymerization of actin into filaments can push membranes forming extensions like filopodia or lamellipodia, which are important during processes such as cell motility and phagocytosis. Similarly, small organelles or pathogens can be moved by actin polymerization. Such actin filaments can be arranged in different patterns and are usually hundreds of nanometers in length as revealed by various electron microscopy approaches. Much shorter actin filaments are involved in the motility of apicomplexan parasites. However, these short filaments have to date not been visualized in intact cells. Here, we investigated Plasmodium sporozoites, the motile forms of the malaria parasite that are transmitted by the mosquito, using cryogenic electron tomography. We detected filopodia-like extensions of the plasma membrane and observed filamentous structures in the supra-alveolar space underneath the plasma membrane. However, these filaments could not be unambiguously assigned as actin filaments. In silico simulations of EM data collection and tomographic reconstruction identify the limits in revealing the filaments due to their length, concentration and orientation.PACS Codes: 87.64.Ee.

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