轴突输运模型中PDMS密封封闭微管阵列上q点分布的转变

K. Fujimoto, H. Shintaku, H. Kotera, R. Yokokawa
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引用次数: 0

摘要

在本文中,我们展示了一个三维(3D)封闭通道中运动蛋白驱动的运输系统的重建,其尺度类似于轴突。我们的实验方法成功地实现了封闭通道中微管(MTs)上大量激酶标记的q点的运动性。为了控制运动蛋白的运动方向,我们在通道中制备了一个极性定义的MT阵列。由于运动蛋白的定向运动性,在封闭通道的一端,即微管(MT) +端,观察到转运q点的时间演化积累。这是构建基于运动蛋白主动转运体外模型的第一步,该模型具有模拟细胞内环境的三维空间约束,适用于分析细胞内转运的调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transition of Q-dot distribution on microtubule array enclosed by PDMS sealing for axonal transport model
In this paper, we show a reconstruction of kinesin driven transport system in three dimensionally (3D) enclosed channels whose scale is similar to axons. Our experimental method enabled successful motility of a large number of kinesin-labeled Q-dots on microtubules (MTs) in enclosed channels. To control the direction of kinesin motility, we prepared a polarity-defined MT array in channels. Due to the directional motility of kinesin, time evolutional accumulation of transported Q-dot at one end of enclosed channels, where corresponds to microtubule (MT) plus end, was observed. This is the first step for an in vitro model of motor protein-based active transport with a 3D spatial confinement mimicking intracellular environment, which is applicable to analyze a regulation mechanism of intracellular transport.
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