Leenders Miriam, Gerwin Claudia, Sheng Zu-Hang
National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Curr Protoc Neurosci. 2004 Sep;Chapter 2:Unit 2.7. doi: 10.1002/0471142301.ns0207s28.
Investigation of synaptic vesicle membrane proteins using multidisciplinary approaches, particularly to characterize synaptic vesicle proteins in synapses, can greatly advance our knowledge of the molecular mechanisms involved in synaptic vesicle exocytosis and neurotransmission. Three approaches are presented in this unit to identify and characterize synaptic vesicle proteins. The first is a subcellular fractionation method used to isolate synaptic vesicles from rat brain synaptosomal preparations, which can then be used in a variety of biochemical studies on synaptic vesicle proteins. The second is a detailed procedure for pre-embedding immunogold staining and electron microscopic observation, techniques that permit the morphological identification of synaptic vesicle proteins in individual vesicles at the intact synapse. Finally, a protocol for immunocytochemical staining of cultured hippocampal neurons for light microscopic examination is provided, which allows one to stain multisynaptic vesicle proteins and determine their localization in relation to other proteins or subcellular structures in synapses.
使用多学科方法研究突触小泡膜蛋白,特别是在突触中表征突触小泡蛋白,能够极大地推进我们对突触小泡胞吐作用和神经传递所涉及分子机制的认识。本单元介绍了三种鉴定和表征突触小泡蛋白的方法。第一种是亚细胞分级分离法,用于从大鼠脑突触体制剂中分离突触小泡,然后可将其用于对突触小泡蛋白进行各种生化研究。第二种是预包埋免疫金染色和电子显微镜观察的详细程序,这些技术能够在完整突触的单个小泡中对突触小泡蛋白进行形态学鉴定。最后,提供了一种用于培养海马神经元免疫细胞化学染色以进行光学显微镜检查的方案,该方案可使人们对多突触小泡蛋白进行染色,并确定它们相对于突触中其他蛋白或亚细胞结构的定位。