Laboratory of Tropical Crop Improvement, Department of Biosystems, K.U. Leuven, Kasteelpark Arenberg 13, PO box 2455, B-3001 Heverlee, Belgium.
J Proteomics. 2011 Aug 12;74(8):1218-29. doi: 10.1016/j.jprot.2011.02.008. Epub 2011 Feb 19.
Membrane proteins are an interesting class of proteins because of their functional importance. Unfortunately their analysis is hampered by low abundance and poor solubility in aqueous media. Since shotgun methods are high-throughput and partly overcome these problems, they are preferred for membrane proteomics. However, their application in non-model plants demands special precautions to prevent false positive identification of proteins. In the current paper, a workflow for membrane proteomics in banana, a poorly sequenced plant, is proposed. The main steps of this workflow are (i) optimization of the peptide separation, (ii) performing de novo sequencing to allow a sequence homology search and (iii) visualization of identified peptide-protein associations using Cytoscape to remove redundancy and wrongly assigned peptides, based on species-specific information. By applying this workflow, integral plasma membrane proteins from banana leaves were successfully identified.
膜蛋白因其功能重要性而成为一类有趣的蛋白质。然而,由于其丰度低且在水介质中溶解度差,其分析受到阻碍。由于鸟枪法方法具有高通量的特点,并在一定程度上克服了这些问题,因此它们更适合用于膜蛋白质组学研究。然而,它们在非模式植物中的应用需要特别注意,以防止错误地鉴定蛋白质。在当前的论文中,提出了一种用于香蕉(一种测序较差的植物)膜蛋白质组学的工作流程。该工作流程的主要步骤包括:(i)优化肽分离,(ii)进行从头测序以允许进行序列同源性搜索,以及(iii)使用 Cytoscape 可视化鉴定的肽-蛋白关联,以根据物种特异性信息去除冗余和错误分配的肽。通过应用该工作流程,成功鉴定了来自香蕉叶片的完整质膜蛋白。