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Dissecting the Nanoscale Distributions and Functions of Microtubule-End-Binding Proteins EB1 and ch-TOG in Interphase HeLa Cells

机译:在相间HeLa细胞中解剖微管末端结合蛋白EB1和ch-TOG的纳米级分布和功能

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摘要

Recently, the EB1 and XMAP215/TOG families of microtubule binding proteins have been demonstrated to bind autonomously to the growing plus ends of microtubules and regulate their behaviour in in vitro systems. However, their functional redundancy or difference in cells remains obscure. Here, we compared the nanoscale distributions of EB1 and ch-TOG along microtubules using high-resolution microscopy techniques, and also their roles in microtubule organisation in interphase HeLa cells. The ch-TOG accumulation sites protruded ∼100 nm from the EB1 comets. Overexpression experiments showed that ch-TOG and EB1 did not interfere with each other’s localisation, confirming that they recognise distinct regions at the ends of microtubules. While both EB1 and ch-TOG showed similar effects on microtubule plus end dynamics and additively increased microtubule dynamicity, only EB1 exhibited microtubule-cell cortex attachment activity. These observations indicate that EB1 and ch-TOG regulate microtubule organisation differently via distinct regions in the plus ends of microtubules.
机译:最近,已证明微管结合蛋白的EB1和XMAP215 / TOG家族可以与微管的生长末端自动结合并在体外系统中调节其行为。但是,它们的功能冗余或单元差异仍然不清楚。在这里,我们使用高分辨率显微镜技术比较了EB1和ch-TOG沿微管的纳米级分布,以及它们在相间HeLa细胞中微管组织中的作用。 ch-TOG累积位点从EB1彗星突出约100 nm。过表达实验表明,ch-TOG和EB1不会干扰彼此的定位,从而证实它们可以识别微管末端的不同区域。虽然EB1和ch-TOG对微管加上末端动力学表现出相似的影响,并且微管动力学增加性增加,但只有EB1表现出微管细胞皮层附着活性。这些观察结果表明,EB1和ch-TOG通过微管正端的不同区域不同地调节微管组织。

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