Zhu Yili, Tan Weimin, Lee Wei-Lih
Department of Biological Sciences, Dartmouth College, Hanover, NH 03755, USA.
Bio Protoc. 2018 Dec 5;8(23). doi: 10.21769/BioProtoc.3110.
In this protocol, we describe a simple microscopy-based method to assess the interaction of a microtubule-associated protein (MAP) with microtubules. The interaction between MAP and microtubules is typically assessed by a co-sedimentation assay, which measures the amount of MAP that co-pellets with microtubules by centrifugation, followed by SDS-PAGE analysis of the supernatant and pellet fractions. However, MAPs that form large oligomers tend to pellet on their own during the centrifugation step, making it difficult to assess co-sedimentation. Here we describe a microscopy-based assay that measures microtubule binding by direct visualization using fluorescently-labeled MAP, solving the limitations of the co-sedimentation assay. Additionally, we recently reported quantification of microtubule bundling by measuring the thickness of individual microtubule structures observed in the microscopy-based assay, making the protocol more advantageous than the traditional microtubule co-pelleting assay.
在本实验方案中,我们描述了一种基于显微镜的简单方法,用于评估微管相关蛋白(MAP)与微管之间的相互作用。MAP与微管之间的相互作用通常通过共沉降分析来评估,该分析通过离心测量与微管共沉淀的MAP量,然后对上清液和沉淀部分进行SDS-PAGE分析。然而,形成大寡聚体的MAP在离心步骤中往往会自行沉淀,这使得评估共沉降变得困难。在这里,我们描述了一种基于显微镜的分析方法,该方法通过使用荧光标记的MAP直接可视化来测量微管结合,解决了共沉降分析的局限性。此外,我们最近报告了通过测量在基于显微镜的分析中观察到的单个微管结构的厚度来量化微管束,使得该实验方案比传统的微管共沉淀分析更具优势。