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实时成像体外单 γTuRC 介导的微管成核事件通过 TIRF 显微镜。

Real-Time Imaging of Single γTuRC-Mediated Microtubule Nucleation Events In Vitro by TIRF Microscopy.

机构信息

The Francis Crick Institute, London, UK.

Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.

出版信息

Methods Mol Biol. 2022;2430:315-336. doi: 10.1007/978-1-0716-1983-4_21.

Abstract

The γ-tubulin ring complex (γTuRC) is the major microtubule nucleator in cells. How γTuRC nucleates microtubules, and how nucleation is regulated is not understood. To gain an understanding of γTuRC activity and regulation at the molecular level, it is important to measure quantitatively how γTuRC interacts with tubulin and potential regulators in space and time. Here, we describe a total internal reflection fluorescence microscopy-based assay on chemically functionalized glass slides for the in vitro study of surface immobilized purified γTuRC. The assay allows to measure microtubule nucleation by γTuRC in real time and at a single molecule level over a wide variety of assay conditions, in the absence and presence of potential regulators. This setup provides a previously unavailable opportunity for quantitative studies of the kinetics of microtubule nucleation by γTuRC.

摘要

γ-微管蛋白环复合物(γTuRC)是细胞中主要的微管核形成物。γTuRC 如何引发微管以及如何调节核形成尚不清楚。为了在分子水平上了解 γTuRC 的活性和调节,定量测量 γTuRC 与微管和潜在调节剂在空间和时间上的相互作用非常重要。在这里,我们描述了一种基于全内反射荧光显微镜的在化学功能化玻片上的体外实验方法,用于研究表面固定化纯化的 γTuRC。该测定法可在广泛的测定条件下,实时和单分子水平测量 γTuRC 引发微管的核形成,而无需和存在潜在调节剂的情况下均可进行。该设置为定量研究 γTuRC 引发微管核形成的动力学提供了以前无法获得的机会。

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