Nitzsche Bert, Ruhnow Felix, Diez Stefan
Nat Nanotechnol. 2008 Sep;3(9):552-6. doi: 10.1038/nnano.2008.216. Epub 2008 Aug 10.
Owing to their wide spectrum of in vivo functions, motor proteins, such as kinesin-1, show great potential for application as nanomachines in engineered environments. When attached to a substrate surface, these motors are envisioned to shuttle cargo that is bound to reconstituted microtubules--one component of the cell cytoskeleton--from one location to another. One potentially serious problem for such applications is, however, the rotation of the microtubules around their longitudinal axis. Here we explore this issue by labelling the gliding microtubules with quantum dots to simultaneously follow their sinusoidal side-to-side and up-and-down motion in three dimensions with nanometre accuracy. Microtubule rotation, which originates from the kinesin moving along the individual protofilaments of the microtubule, was not impeded by the quantum dots. However, pick-up of large cargo inhibited the rotation but did not affect the velocity of microtubule gliding. Our data show that kinesin-driven microtubules make flexible, responsive and effective molecular shuttles for nanotransport applications.
由于其在体内具有广泛的功能,驱动蛋白-1等驱动蛋白在工程环境中作为纳米机器具有巨大的应用潜力。当附着在底物表面时,这些马达被设想为将与重组微管(细胞骨架的一个组成部分)结合的货物从一个位置运送到另一个位置。然而,此类应用中一个潜在的严重问题是微管围绕其纵轴的旋转。在这里,我们通过用量子点标记滑动的微管来探索这个问题,以便在三维空间中以纳米精度同时跟踪它们的正弦左右和上下运动。微管旋转源于驱动蛋白沿着微管的各个原纤维移动,量子点并未阻碍这种旋转。然而,搭载大型货物会抑制旋转,但不会影响微管滑动的速度。我们的数据表明,驱动蛋白驱动的微管为纳米运输应用提供了灵活、响应迅速且有效的分子穿梭工具。