Moores Carolyn A, Perderiset Mylène, Francis Fiona, Chelly Jamel, Houdusse Anne, Milligan Ronald A
Department of Cell Biology, CB227, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Mol Cell. 2004 Jun 18;14(6):833-9. doi: 10.1016/j.molcel.2004.06.009.
Neurons undertake an amazing journey from the center of the developing mammalian brain to the outer layers of the cerebral cortex. Doublecortin, a component of the microtubule cytoskeleton, is essential in postmitotic neurons and was identified because its mutation disrupts human brain development. Doublecortin stabilizes microtubules and stimulates their polymerization but has no homology with other MAPs. We used electron microscopy to characterize microtubule binding by doublecortin and visualize its binding site. Doublecortin binds selectively to 13 protofilament microtubules, its in vivo substrate, and also causes preferential assembly of 13 protofilament microtubules. This specificity was explained when we found that doublecortin binds between the protofilaments from which microtubules are built, a previously uncharacterized binding site that is ideal for microtubule stabilization. These data reveal the structural basis for doublecortin's binding selectivity and provide insight into its role in maintaining microtubule architecture in maturing neurons.
神经元在发育中的哺乳动物大脑中经历了一段从中心到大脑皮质外层的惊人旅程。双皮质素是微管细胞骨架的一个组成部分,在有丝分裂后的神经元中至关重要,它因突变会破坏人类大脑发育而被发现。双皮质素能稳定微管并刺激其聚合,但与其他微管相关蛋白无同源性。我们利用电子显微镜来表征双皮质素与微管的结合,并可视化其结合位点。双皮质素选择性地结合到13根原纤维微管上,这是其在体内的底物,并且还会促使13根原纤维微管优先组装。当我们发现双皮质素结合在构成微管的原纤维之间时,这种特异性就得到了解释,这是一个以前未被描述的结合位点,非常适合微管稳定。这些数据揭示了双皮质素结合选择性的结构基础,并为其在成熟神经元中维持微管结构的作用提供了见解。