Biophysics, BIOTEC, Technische Universität Dresden, Tatzberg 47/49, 01307 Dresden, Germany.
Chemphyschem. 2012 Mar;13(4):1001-6. doi: 10.1002/cphc.201100669. Epub 2011 Dec 23.
We report on a minimal system to mimic intracellular transport of membrane-bounded, vesicular cargo. In a cell-free assay, purified kinesin-1 motor proteins were directly anchored to the membrane of giant unilamellar vesicles, and their movement studied along two-dimensional microtubule networks. Motion-tracking of vesicles with diameters of 1-3 μm revealed traveling distances up to the millimeter range. The transport velocities were identical to velocities of cargo-free motors. Using total internal reflection fluorescence (TIRF) microscopy, we were able to estimate the number of GFP-labeled motors involved in the transport of a single vesicle. We found that the vesicles were transported by the cooperative activity of typically 5-10 motor molecules. The presented assay is expected to open up further applications in the field of synthetic biology, aiming at the in vitro reconstitution of sub-cellular multi-motor transport systems. It may also find applications in bionanotechnology, where the controlled long-range transport of artificial cargo is a promising means to advance current lab-on-a-chip systems.
我们报告了一个最小的系统,用于模拟细胞内膜结合的囊泡货物的运输。在无细胞测定中,纯化的驱动蛋白-1 马达蛋白直接锚定在巨大的单层囊泡的膜上,并沿着二维微管网络研究它们的运动。直径为 1-3 μm 的囊泡的运动追踪显示,其移动距离可达毫米级。运输速度与无货物的马达速度相同。使用全内反射荧光(TIRF)显微镜,我们能够估计参与单个囊泡运输的 GFP 标记马达的数量。我们发现,囊泡是通过通常 5-10 个马达分子的协同活性来运输的。所提出的测定方法有望在合成生物学领域开辟进一步的应用,旨在体外重建亚细胞多马达运输系统。它也可能在生物纳米技术中找到应用,在生物纳米技术中,人工货物的受控远程运输是推进当前芯片实验室系统的有前途的手段。