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驱动蛋白驱动的分子穿梭机从工程化装载站拾取货物。

Cargo pick-up from engineered loading stations by kinesin driven molecular shuttles.

作者信息

Brunner Christian, Wahnes Christian, Vogel Viola

机构信息

Laboratory for Biologically Oriented Materials, Department of Materials, ETH Zürich, Hönggerberg, CH-8093, Zürich, Switzerland.

出版信息

Lab Chip. 2007 Oct;7(10):1263-71. doi: 10.1039/b707301a. Epub 2007 Jul 25.

Abstract

Exploiting biological motors ex vivo to transport and distribute cargo with high spatial control, as done by cells, requires that we learn how molecular shuttles (microtubules propelled by kinesins) can pick up cargo from defined surface regions (loading stations). The main challenge of building microfabricated cargo loading stations is to adjust the sum of non-covalent interactions such that the station stably holds on to the cargo under static conditions, but allows for transfer when a gliding microtubule collides with station-bound cargo and starts to pull on it. Successful pick-up of cargo could be observed using biotin-anti-biotin interactions and hybridized oligonucleotides. The effect of different tethering chemistries on the efficiency of cargo pick-up was tested.

摘要

如细胞所做的那样,在体外利用生物马达以高度的空间控制来运输和分配货物,这要求我们了解分子穿梭器(由驱动蛋白推动的微管)如何从特定表面区域(装载站)拾取货物。构建微纳加工货物装载站的主要挑战在于调整非共价相互作用的总和,使得该装载站在静态条件下能稳定地固定住货物,但当滑动的微管与固定在装载站上的货物碰撞并开始拉动它时,又能允许货物转移。利用生物素-抗生物素相互作用和杂交寡核苷酸,可以观察到货物的成功拾取。测试了不同连接化学对货物拾取效率的影响。

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