通过改变表面电荷密度来控制电场中的微管轨迹(11)。分子马达,海报,第52届日本生物物理学会年会(BSJ2014)

N. Isozaki, S. Ando, H. Shintaku, H. Kotera, E. Meyhofer, R. Yokokawa
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引用次数: 1

摘要

在功能性纳米系统中使用由马达驱动的微管(MTs)面临的挑战是如何控制它们的运动方向。通过链亲和素-生物素相互作用,设计带有dsDNA标记的MT负端带电表面,开发了一种在电场下引导运动蛋白驱动的MT多向运动的方法。实验轨迹与电泳迁移率的预测值非常吻合。由于标记的DNA分子的有效电荷与自由分散的DNA分子的有效电荷相匹配,因此即使选择已知电荷的标记分子,也可以估计出MT轨迹。我们的分子设计和预测方法证明了使用由运动蛋白驱动的分子分选器的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
3P145 Control of microtubule trajectory within an electric field by altering surface charge density(11. Molecular motor,Poster,The 52nd Annual Meeting of the Biophysical Society of Japan(BSJ2014))
A challenge for using microtubules (MTs) driven by kinesin motors in functional nanosystems is to control their direction of movement. A method was developed to guide kinesin-propelled MTs in multiple directions under an electric field by designing a charged surface of MT minus ends labeled with dsDNA via a streptavidin-biotin interaction. Experimental trajectories were in good agreement with values predicted from measured electrophoretic mobilities. As the effective charge of labeled DNA molecules matches to that of freely dispersed DNA molecules, MT trajectory can be estimated even by selecting labeling molecules with known charges. Our molecular design and prediction methodology demonstrate the feasibility of using molecular sorters driven by motor proteins.
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