Magiera Maria M, Janke Carsten
Institut Curie, CNRS UMR3306, INSERM U1005, Orsay, France.
Methods Cell Biol. 2013;115:247-67. doi: 10.1016/B978-0-12-407757-7.00016-5.
Microtubules play highly diverse and essential roles in every eukaryotic cell. While built from conserved dimers of α- and β-tubulin, microtubules can be diversified by posttranslational modifications in order to fulfill specific functions in cells. The tubulin posttranslational modifications: acetylation, detyrosination, polyglutamylation, and polyglycylation play important roles in microtubule functions; however, only little functional and mechanistic insight has been gained so far. The modification state of microtubules can be visualized with specific antibodies. A drawback is that detailed information about the specificities and limitations of these antibodies are not easily accessible in the literature. We provide here a comprehensive description of the currently available set of antibodies specific to tubulin modifications. Focusing on glutamylation antibodies, we discuss specific protocols that allow using these antibodies to gain semi-quantitative information on the levels and distribution of tubulin modifications in immunocytochemistry and immunoblot.
微管在每个真核细胞中发挥着高度多样且至关重要的作用。微管由α-和β-微管蛋白的保守二聚体构建而成,可通过翻译后修饰实现多样化,以便在细胞中履行特定功能。微管蛋白的翻译后修饰,如乙酰化、去酪氨酸化、多聚谷氨酰胺化和多聚糖基化,在微管功能中发挥着重要作用;然而,到目前为止,我们对其功能和机制的了解还很少。微管的修饰状态可用特异性抗体进行可视化。一个缺点是,关于这些抗体的特异性和局限性的详细信息在文献中并不容易获取。我们在此全面描述了目前可用的一组针对微管蛋白修饰的抗体。以谷氨酰胺化抗体为重点,我们讨论了特定的方案,这些方案可使我们利用这些抗体在免疫细胞化学和免疫印迹中获得关于微管蛋白修饰水平和分布的半定量信息。