Max Planck Institute of Psychiatry, Proteomics and Biomarkers, Munich, Germany.
Electrophoresis. 2010 Apr;31(8):1294-301. doi: 10.1002/elps.200900647.
Synapses play important roles in neurotransmission and neuroplasticity. For an in-depth analysis of the synaptic proteome and phosphoproteome, synaptosomal proteins from whole mouse brain were analyzed by IEF and MS resulting in the largest synaptosome proteome described to date, with 2980 unique proteins identified with two or more peptides. At the same time, 118 synaptosomal phosphoproteins were identified, eight of which are reported for the first time as phosphorylated. Expression of selected proteins in synaptosomes was investigated by Western blot. We demonstrate that IEF is a powerful method to interrogate complex samples such as brain tissue both at the proteome and the phosphoproteome level without the need of additional enrichment for phosphoproteins. The detailed synaptoproteome data set reported here will help to elucidate the molecular complexity of the synapse and contribute to our understanding of synaptic systems biology in health and disease.
突触在神经传递和神经可塑性中发挥着重要作用。为了深入分析突触蛋白组和磷酸化蛋白组,我们使用 IEF 和 MS 分析了来自整个小鼠大脑的突触体蛋白,得到了迄今为止最大的突触体蛋白质组描述,其中有 2980 种独特的蛋白质被鉴定出有两个或更多的肽。同时,鉴定到 118 种突触体磷酸化蛋白,其中 8 种是首次被报道为磷酸化的。通过 Western blot 研究了突触体中选定蛋白质的表达。我们证明IEF 是一种强大的方法,可以在蛋白质组和磷酸化蛋白质组水平上对复杂的样本(如脑组织)进行分析,而无需对磷酸化蛋白进行额外的富集。这里报告的详细突触蛋白质组数据集将有助于阐明突触的分子复杂性,并有助于我们理解健康和疾病中的突触系统生物学。