Reid Taylor A, Coombes Courtney, Gardner Melissa K
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA
Biol Open. 2017 Aug 15;6(8):1245-1256. doi: 10.1242/bio.025320.
Microtubules are structural polymers that participate in a wide range of cellular functions. The addition and loss of tubulin subunits allows the microtubule to grow and shorten, as well as to develop and repair defects and gaps in its cylindrical lattice. These lattice defects act to modulate the interactions of microtubules with molecular motors and other microtubule-associated proteins. Therefore, tools to control and measure microtubule lattice structure will be invaluable for developing a quantitative understanding of how the structural state of the microtubule lattice may regulate its interactions with other proteins. In this work, we manipulated the lattice integrity of microtubules to create pools of microtubules with common nucleotide states, but with variations in structural states. We then developed a series of novel semi-automated analysis tools for both fluorescence and electron microscopy experiments to quantify the type and severity of alterations in microtubule lattice integrity. These techniques will enable new investigations that explore the role of microtubule lattice structure in interactions with microtubule-associated proteins.
微管是参与多种细胞功能的结构聚合物。微管蛋白亚基的添加和丢失使微管能够生长和缩短,以及在其圆柱形晶格中形成和修复缺陷及间隙。这些晶格缺陷起到调节微管与分子马达及其他微管相关蛋白相互作用的作用。因此,控制和测量微管晶格结构的工具对于定量理解微管晶格的结构状态如何调节其与其他蛋白的相互作用将非常宝贵。在这项工作中,我们操纵微管的晶格完整性,以创建具有共同核苷酸状态但结构状态不同的微管池。然后,我们为荧光和电子显微镜实验开发了一系列新颖的半自动分析工具,以量化微管晶格完整性改变的类型和严重程度。这些技术将使新的研究能够探索微管晶格结构在与微管相关蛋白相互作用中的作用。