Sialana Fernando J, Gulyassy Peter, Májek Peter, Sjöstedt Evelina, Kis Viktor, Müller André C, Rudashevskaya Elena L, Mulder Jan, Bennett Keiryn L, Lubec Gert
Department of Pharmaceutical Chemistry, University of Vienna, Vienna, Austria.
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Proteomics. 2016 Nov;16(22):2911-2920. doi: 10.1002/pmic.201600234.
The molecular composition of synaptic signal transduction machineries shapes synaptic neurotransmission. The repertoire of receptors, transporters and channels (RTCs) comprises major signaling events in the brain. RTCs are conventionally studied by candidate immunohistochemistry and biochemistry, which are low throughput with resolution greatly affected by available immunoreagents and membrane interference. Therefore, a comprehensive resource of synaptic brain RTCs is still lacking. In particular, studies on the detergent-soluble synaptosomal fraction, known to contain transporters and channels, are limited. We, therefore, performed sub-synaptosomal fractionation of rat cerebral cortex, followed by trypsin/chymotrypsin sequential digestion of a detergent-soluble synaptosomal fraction and a postsynaptic density preparation, stable-isotope tryptic peptide labeling and liquid chromatography mass spectrometry. Based on the current study, a total of 4784 synaptic proteins were submitted to the ProteomExchange database (PXD001948), including 274 receptors, 394 transporters/channels and 1377 transmembrane proteins. Function-based classification assigned 1781 proteins as probable drug targets with 834 directly linked to brain disorders. The analytical approach identified 499 RTCs that are not listed in the largest, curated database for synaptosomal proteins (SynProt). This is a threefold RTC increase over all other data collected to date. Taken together, we present a protein discovery resource that can serve as a benchmark for future molecular interrogation of synaptic connectivity.
突触信号转导机制的分子组成塑造了突触神经传递。受体、转运体和通道(RTCs)的全部组成包括大脑中的主要信号事件。传统上,RTCs是通过候选免疫组织化学和生物化学方法进行研究的,这些方法通量较低,分辨率受可用免疫试剂和膜干扰的影响很大。因此,目前仍缺乏关于突触脑RTCs的全面资源。特别是,对已知含有转运体和通道的去污剂可溶性突触体部分的研究有限。因此,我们对大鼠大脑皮层进行了亚突触体分级分离,随后对去污剂可溶性突触体部分和突触后致密体制剂进行胰蛋白酶/糜蛋白酶顺序消化、稳定同位素胰蛋白酶肽标记和液相色谱质谱分析。基于当前的研究,共有4784种突触蛋白被提交到蛋白质组交换数据库(PXD001948),其中包括274种受体、394种转运体/通道和1377种跨膜蛋白。基于功能的分类将1781种蛋白质指定为可能的药物靶点,其中834种与脑部疾病直接相关。该分析方法鉴定出499种未在最大的、经过整理的突触体蛋白数据库(SynProt)中列出的RTCs。这比迄今为止收集的所有其他数据中的RTCs数量增加了两倍。综上所述,我们提供了一种蛋白质发现资源,可作为未来对突触连接性进行分子研究的基准。