Lee Woei Ming, Reece Peter J, Marchington Robert F, Metzger Nikolaus K, Dholakia Kishan
SUPA, School of Physics and Astronomy, University of St. Andrews, North Haugh, St. Andrews KY16 9SS, UK.
Nat Protoc. 2007;2(12):3226-38. doi: 10.1038/nprot.2007.446.
The application of optical traps has come to the fore in the last three decades. They provide a powerful, sterile and noninvasive tool for the manipulation of cells, single biological macromolecules, colloidal microparticles and nanoparticles. An optically trapped microsphere may act as a force transducer that is used to measure forces in the piconewton regime. By setting up a well-calibrated single-beam optical trap within a fluorescence microscope system, one can measure forces and collect fluorescence signals upon biological systems simultaneously. In this protocol, we aim to provide a clear exposition of the methodology of assembling and operating a single-beam gradient force trap (optical tweezers) on an inverted fluorescence microscope. A step-by-step guide is given for alignment and operation, with discussion of common pitfalls.
在过去三十年中,光镊的应用已崭露头角。它们为操控细胞、单个生物大分子、胶体微粒和纳米颗粒提供了一种强大、无菌且无创的工具。一个被光镊捕获的微球可作为一个力传感器,用于测量皮牛顿量级的力。通过在荧光显微镜系统内设置一个校准良好的单光束光镊,人们可以同时测量生物系统上的力并收集荧光信号。在本实验方案中,我们旨在清晰阐述在倒置荧光显微镜上组装和操作单光束梯度力阱(光镊)的方法。给出了对准和操作的分步指南,并讨论了常见的陷阱。