Aradska Jana, Bulat Tanja, Sialana Fernando J, Birner-Gruenberger Ruth, Erich Buchner, Lubec Gert
Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
Institute of Pathology, Medical University of Graz, Core Facility Mass Spectrometry, Center for Medical Research, BioTechMed Omics Center Graz, Graz, Austria.
Proteomics. 2015 Oct;15(19):3356-60. doi: 10.1002/pmic.201500092. Epub 2015 Sep 10.
Membrane proteins play key roles in several fundamental biological processes such as cell signalling, energy metabolism and transport. Despite the significance, these still remain an under-represented group in proteomics datasets. Herein, a bottom-up approach to analyse an enriched membrane fraction from Drosophila melanogaster heads using multidimensional liquid chromatography (LC) coupled with tandem-mass spectrometry (MS/MS) that relies on complete solubilisation and digestion of proteins, is reported. An enriched membrane fraction was prepared using equilibrium density centrifugation on a discontinuous sucrose gradient, followed by solubilisation using the filter-aided sample preparation (FASP), tryptic and sequential chymotryptic digestion of proteins. Peptides were separated by reversed-phase (RP) LC at high pH in the first dimension and acidic RP-LC in the second dimension coupled directly to an Orbitrap Velos Pro mass spectrometer. A total number of 4812 proteins from 114 865 redundant and 38 179 distinct peptides corresponding to 4559 genes were identified in the enriched membrane fraction from fly heads. These included brain receptors, transporters and channels that are most important elements as drug targets or are linked to disease. Data are available via ProteomeXchange with identifier PXD001712 (http://proteomecentral.proteomexchange.org/dataset/PXD001712).
膜蛋白在细胞信号传导、能量代谢和运输等若干基本生物学过程中发挥着关键作用。尽管其具有重要意义,但在蛋白质组学数据集中,这些蛋白仍然是代表性不足的一类。本文报道了一种自下而上的方法,该方法使用多维液相色谱(LC)与串联质谱(MS/MS)联用,对黑腹果蝇头部的富集膜组分进行分析,该方法依赖于蛋白质的完全溶解和消化。使用不连续蔗糖梯度平衡密度离心法制备富集膜组分,随后使用滤膜辅助样品制备(FASP)进行溶解,对蛋白质进行胰蛋白酶消化和顺序胰凝乳蛋白酶消化。肽段在第一维通过高pH值的反相(RP)LC进行分离,在第二维通过酸性RP-LC进行分离,并直接与Orbitrap Velos Pro质谱仪联用。在果蝇头部的富集膜组分中,共鉴定出4812种蛋白质,它们来自114865条冗余肽段和38179条对应于4559个基因的独特肽段。这些蛋白质包括作为药物靶点或与疾病相关的最重要的脑受体、转运蛋白和通道。数据可通过ProteomeXchange获得,标识符为PXD001712(http://proteomecentral.proteomexchange.org/dataset/PXD001712)。