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Surface topography of microtubule walls decorated with monomeric and dimeric kinesin constructs

机译:微管内壁的表面形貌饰有单体和二聚体驱动蛋白结构

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摘要

The surface topography of opened-up microtubule walls (sheets) decorated with monomeric and dimeric kinesin motor domains was investigated by freeze-drying and unidirectional metal shadowing. Electron microscopy of surface-shadowed specimens produces images with a high signal/noise ratio, which enable a direct observation of surface features below 2 nm detail. Here we investigate the inner and outer surface of microtubules and tubulin sheets with and without decoration by kinesin motor domains. Tubulin sheets are flattened walls of microtubules, keeping lateral protofilament contacts intact. Surface shadowing reveals the following features: (i) when the microtubule outside is exposed the surface relief is dominated by the bound motor domains. Monomeric motor constructs generate a strong 8 nm periodicity, corresponding to the binding of one motor domain per beta -tubulin heterodimer. This surface periodicity largely disappears when dimeric kinesin motor domains are used for decoration, even though it is still visible in negatively stained or frozen hydrated specimens, This could be explained by disorder in the binding of the second (loosely tethered) kinesin head, and/or disorder in the coiled-coil tail. (ii) Both surfaces of undecorated sheets or microtubules, as well as the inner surface of decorated sheets, reveal a strong 4 nm repeat (due to the periodicity of tubulin monomers) and a weak 8 nm repeat (due to slight differences between alpha- and beta -tubulin). The differences between alpha- and beta -tubulin on the inner surface are stronger than expected from cryo-electron microscopy of unstained microtubules, indicating the existence of tubulin subdomain-specific surface properties that reflect the surface corrugation and hence metal deposition during evaporation. The 16 nm periodicity visible in some negatively stained specimens (caused by the pairing of cooperatively bound kinesin dimers) is not detected by surface shadowing.
机译:通过冷冻干燥和单向金属遮蔽研究了用单体和二聚体驱动蛋白运动域装饰的开放微管壁(片)的表面形貌。表面阴影标本的电子显微镜可产生具有高信噪比的图像,从而可以直接观察2 nm以下细节的表面特征。在这里,我们调查的微管和微管蛋白片的内表面和外表面有和没有驱动蛋白运动域的装饰。小管蛋白片是微管的扁平壁,可保持原丝的侧向接触完整。表面阴影显示出以下特征:(i)当外部微管暴露时,表面起伏主要由结合的运动域控制。单体马达构建体产生强的8 nm周期性,对应于每个β-微管蛋白异二聚体结合一个马达域。当使用二聚驱动蛋白驱动结构域进行装饰时,即使在负染色或冷冻的水合标本中仍然可见,这种表面周期性在很大程度上消失了,这可以解释为第二个(松散连接的)驱动蛋白头的结合无序,和/或盘绕线圈尾部的混乱。 (ii)未经修饰的薄板或微管的两个表面,以及装饰薄板的内表面,都显示出强4 nm重复(由于微管蛋白单体的周期性)和弱8 nm重复(由于α-之间的细微差异)和β-微管蛋白)。内表面上的α-微管蛋白和β-微管蛋白之间的差异比未染色微管的冷冻电子显微镜所预期的要强,表明存在微管蛋白亚结构域特定的表面特性,这些表面特性反映了表面波纹,从而反映了蒸发过程中的金属沉积。在某些负染色的样品中可见的16 nm周期性(由协同结合的驱动蛋白二聚体配对引起)无法通过表面阴影检测到。

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