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单枪匹马:通过用于全内反射荧光显微镜的体外测定法测量微管的运动

Going solo: measuring the motions of microtubules with an in vitro assay for TIRF microscopy.

作者信息

Leslie Kris, Galjart Niels

机构信息

Department of Cell Biology, Erasmus Medical Center, P.O. Box 2040, Rotterdam, The Netherlands.

出版信息

Methods Cell Biol. 2013;115:109-24. doi: 10.1016/B978-0-12-407757-7.00008-6.

Abstract

Microtubule (MT) plus-end-tracking proteins (+TIPs) specifically associate with the plus ends of growing MTs, thereby determining, in many different ways, the dynamic behavior of the MTs. Over the past years, a variety of fluorescently tagged +TIPs have been purified. Their reconstitution together with other purified components involved in MT plus-end-tracking, and analysis by total internal reflection fluorescence microscopy, has helped to elucidate some of the crucial mechanisms underlying the motion of MTs. For example, +TIP dwell time and association rate, and key MT dynamic instability parameters can be measured in a controlled cell-free environment. In this chapter, we have aimed to describe in an accessible and practical manner how we carry out these assays in our lab. We cover basic steps such as the preparation of glass and sample chambers through to the details of the in vitro +TIP assay. When appropriate, we mention common problems providing practical help to overcome potential issues.

摘要

微管(MT)正端追踪蛋白(+TIPs)特异性地与生长中的微管正端结合,从而以多种不同方式决定微管的动态行为。在过去几年中,多种荧光标记的+TIPs已被纯化。将它们与参与微管正端追踪的其他纯化成分一起重组,并通过全内反射荧光显微镜进行分析,有助于阐明微管运动背后的一些关键机制。例如,可以在可控的无细胞环境中测量+TIP的驻留时间和结合速率,以及关键的微管动态不稳定性参数。在本章中,我们旨在以易懂且实用的方式描述我们在实验室中如何进行这些测定。我们涵盖了从玻璃和样品室的制备到体外+TIP测定细节等基本步骤。在适当的时候,我们会提及常见问题,并提供实际帮助以克服潜在问题。

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