Diez Stefan, Schief William R, Howard Jonathon
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstr. 108, 01307 Dresden, Germany.
Curr Biol. 2002 Mar 19;12(6):R203-5. doi: 10.1016/s0960-9822(02)00750-9.
A fusion protein of kinesin and gelsolin binds a short actin filament which can be visualized using a standard fluorescence microscope. This technique has provided new insight into the mechanism of kinesin action, and in principle it can be extended to allow single-molecule assays of any protein.
驱动蛋白和凝溶胶蛋白的融合蛋白结合了一条短肌动蛋白丝,使用标准荧光显微镜即可观察到。这项技术为驱动蛋白的作用机制提供了新的见解,原则上它可以扩展到对任何蛋白质进行单分子分析。