Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Biomolecules. 2023 Jun 16;13(6):998. doi: 10.3390/biom13060998.
In the last two decades, our knowledge of synaptic proteomes and their relationship to normal brain function and neuropsychiatric disorders has been expanding rapidly through the use of more powerful neuroproteomic approaches. However, mass spectrometry (MS)-based neuroproteomic studies of synapses still require cell-type, spatial, and temporal proteome information. With the advancement of sample preparation and MS techniques, we have just begun to identify and understand proteomes within a given cell type, subcellular compartment, and cell-type-specific synapse. Here, we review the progress and limitations of MS-based neuroproteomics of synapses in the mammalian CNS and highlight the recent applications of these approaches in studying neuropsychiatric disorders such as major depressive disorder and substance use disorders. Combining neuroproteomic findings with other omics studies can generate an in-depth, comprehensive map of synaptic proteomes and possibly identify new therapeutic targets and biomarkers for several central nervous system disorders.
在过去的二十年中,通过使用更强大的神经蛋白质组学方法,我们对突触蛋白质组及其与正常大脑功能和神经精神疾病的关系的了解迅速扩展。然而,基于质谱(MS)的突触神经蛋白质组学研究仍然需要细胞类型、空间和时间蛋白质组信息。随着样品制备和 MS 技术的进步,我们才刚刚开始识别和理解特定细胞类型、亚细胞区室和细胞类型特异性突触内的蛋白质组。在这里,我们回顾了哺乳动物中枢神经系统中基于 MS 的突触神经蛋白质组学的进展和局限性,并强调了这些方法在研究神经精神疾病(如重度抑郁症和物质使用障碍)中的最新应用。将神经蛋白质组学研究结果与其他组学研究相结合,可以生成突触蛋白质组的深入、全面图谱,并可能为几种中枢神经系统疾病确定新的治疗靶点和生物标志物。