J Mol Neurosci. 2014 Mar;52(3):384-91. doi: 10.1007/s12031-013-0162-x.
Neurons establish interactions with target cells via elongation and guidance of axons, and the growth cone plays pivotal roles in this process. Cyclin-dependent kinase 5 (Cdk5)is a key regulator of nervous system development. Cdk5 regulates several significant events by phosphorylating substrates that are involved in neurogenesis, and previous studies of Cdk5 have typically focused on single substrates. Here, we took anew approach to investigate Cdk5 substrates using mass spectrometry and bioinformatics analyses. Axonal growth cones were isolated and analyzed by HPLC-MALDI-MS/MS. In total, 178,617 MS/MS spectra were detected. Candidates were analyzed by GPS 2.1 and Scansite 3, which predicted that 2,664 and 275 sites, respectively, were potential phosphorylation sites of Cdk5. There were 190 overlapped phosphorylation sites, corresponding to 89 proteins. Those proteins correlated with axonal functions were classified, and two of them were verified using a classic site-specific mutation strategy. This is the first study in which the phosphoproteome of axonal growth cones was identified. The systematic examination of Cdk5 substrates could provide a reference for further study of molecular mechanisms of axonal growth cones, and new insights into treatments of neuronal disorders.
神经元通过轴突的延伸和导向与靶细胞建立相互作用,而生长锥在这个过程中起着关键作用。细胞周期蛋白依赖性激酶 5(Cdk5)是神经系统发育的关键调节因子。Cdk5 通过磷酸化参与神经发生的底物来调节几个重要事件,之前对 Cdk5 的研究通常集中在单个底物上。在这里,我们采用了一种新的方法,使用质谱和生物信息学分析来研究 Cdk5 底物。通过 HPLC-MALDI-MS/MS 分离和分析轴突生长锥。总共检测到 178617 个 MS/MS 光谱。通过 GPS 2.1 和 Scansite 3 对候选物进行分析,分别预测 2664 和 275 个位点是 Cdk5 的潜在磷酸化位点。有 190 个重叠的磷酸化位点,对应 89 种蛋白质。与轴突功能相关的那些蛋白质被分类,其中两个使用经典的特异性位点突变策略进行了验证。这是首次鉴定轴突生长锥的磷酸蛋白质组。对 Cdk5 底物的系统检查可以为进一步研究轴突生长锥的分子机制提供参考,并为神经元疾病的治疗提供新的见解。