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Transport and self-organization across different length scales powered by motor proteins and programmed by DNA

机译:由运动蛋白驱动并由DNA编程的不同长度尺度的运输和自组织

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In eukaryotic cells, cargo is transported on self-organized networks of microtubule trackways by kinesin and dynein motor proteins. Synthetic microtubule networks have previously been assembled in vitro, and microtubules have been used as shuttles to carry cargoes on lithographically defined tracks consisting of surface-bound kinesin motors. Here, we show that molecular signals can be used to program both the architecture and the operation of a self-organized transport system that is based on kinesin and microtubules and spans three orders of magnitude in length scale. A single motor protein, dimeric kinesin-1, is conjugated to various DNA nanostructures to accomplish different tasks. Instructions encoded into the DNA sequences are used to direct the assembly of a polar array of microtubules and can be used to control the loading, active concentration and unloading of cargo on this track network, or to trigger the disassembly of the network.
机译:在真核细胞中,货物通过驱动蛋白和动力蛋白的运动蛋白在自组织的微管通道网络上运输。合成的微管网络先前已在体外组装,并且微管已用作穿梭车,以在由表面结合的驱动蛋白马达组成的光刻定义的轨道上运送货物。在这里,我们表明分子信号可用于对基于驱动蛋白和微管的自组织运输系统的体系结构和操作进行编程,并且在长度尺度上跨越三个数量级。单一的运动蛋白,二聚体驱动蛋白1,被缀合到各种DNA纳米结构以完成不同的任务。编码到DNA序列中的指令用于指导微管极性阵列的组装,并可以用于控制该跟踪网络上货物的装载,有效浓度和卸载,或触发网络的拆卸。

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