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首页> 外文期刊>FEBS letters. >Microtubule binding proteins CLIP-170, EB1, and p150Glued form distinct plus-end complexes.
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Microtubule binding proteins CLIP-170, EB1, and p150Glued form distinct plus-end complexes.

机译:微管结合蛋白CLIP-170,EB1和p150Glued形成独特的正端复合物。

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Microtubule plus-end proteins CLIP-170 and EB1 dynamically track the tips of growing microtubules in vivo. Here we examine the association of these proteins with microtubules in vitro. CLIP-170 binds tubulin dimers and co-assembles into growing microtubules. EB1 binds tubulin dimers more weakly, so no co-assembly is observed. However, EB1 binds to CLIP-170, and forms a co-complex with CLIP-170 and tubulin that is recruited to growing microtubule plus ends. The interaction between CLIP-170 and EB1 is competitively inhibited by the related CAP-Gly protein p150Glued, which also localizes to microtubule plus ends in vivo. Based on these observations, we propose a model in which the formation of distinct plus-end complexes may differentially affect microtubule dynamics in vivo.
机译:微管正端蛋白CLIP-170和EB1动态跟踪体内生长的微管的尖端。在这里,我们检查了这些蛋白与微管的体外关联。 CLIP-170结合微管蛋白二聚体并共同组装成正在生长的微管。 EB1与微管蛋白二聚体的结合较弱,因此未观察到共组装。但是,EB1与CLIP-170结合,并与CLIP-170和微管蛋白形成复合物,该复合物被募集到正在生长的微管末端。 CLIP-170和EB1之间的相互作用被相关的CAP-Gly蛋白p150Glued竞争性抑制,p150Glued也定位于体内的微管和末端。基于这些观察,我们提出了一个模型,其中独特的正端复合物的形成可能会差异性地影响体内的微管动力学。

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