Characterisation and Comparability Laboratory, The National Institute for Bioprocessing Research and Training, Foster Avenue, Mount Merrion, Co. Dublin, A94 X099, Ireland; School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 R590, Ireland.
School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 R590, Ireland.
J Chromatogr A. 2018 Sep 7;1566:32-43. doi: 10.1016/j.chroma.2018.06.044. Epub 2018 Jun 19.
Serum remains an attractive source for the discovery of disease related biomarkers due to its intimate interaction with the majority of tissues within the body. The dynamic range of proteins present within serum has long complicated the ability to detect low level tissue leakage proteins that offer more promise as potential biomarkers due to their higher degree of specificity. Depletion strategies, using affinity based sorbents, to remove the most abundant serum proteins are routinely used for matrix simplification during discovery strategies focused on the serum proteome or glycoproteome. Glycoproteins bearing glycans with terminal sialic acid residues have been shown to be differentially expressed in a variety of cancers and are of interest due to the varied involvement of sialic acid in biological functions related to cancer development and metastasis. Herein, we describe the use of 14P serum depletion with subsequent off-gel isoelectric focusing using narrow pH range acidic strips, to facilitate simplification and enrichment of the acidic proteome and glycoproteome prior to label free liquid chromatography mass spectrometry (LC-MS) based proteomic analysis. The developed platform enabled the detection of proteins present within serum at sub-nanomolar concentrations while data analysis using a variety of bioinformatics resources suggested that many of the detected proteins were tissue leakage proteins or proteins associated with specific cellular compartments, rather than traditional secreted proteins. Comparison with theoretical isoelectric point (pI) values also revealed that some detected proteins had higher pI values than the separation range applied during the IEF step, suggesting that their presence may be due to glycans with high degrees of sialylation being attached to the protein backbone, as well as the presence of other post translational modifications. Such findings agree with offline glycomic profiling of the IEF fractions wherein increasing degrees of sialylation were detected across the pH strip from the basic towards the acidic end. Application of the platform using pooled serum from patients bearing gastric cancer, both before and after surgical intervention for tumour removal, revealed a number of differentially expressed proteins associated with cell recognition and cell signalling. The developed platform enabled excellent sensitivity and offers strong potential for application within biomarker discovery studies focused on the acidic proteome.
血清仍然是发现疾病相关生物标志物的有吸引力的来源,因为它与体内大多数组织密切相互作用。由于其更高的特异性,作为潜在生物标志物,低水平组织渗漏蛋白具有更大的潜力,因此,血清中存在的蛋白质的动态范围长期以来一直使检测到这些蛋白质的能力变得复杂。使用基于亲和性的吸附剂的消耗策略来去除最丰富的血清蛋白,通常用于在专注于血清蛋白质组或糖蛋白质组的发现策略中简化基质。带有末端唾液酸残基的糖蛋白已被证明在各种癌症中差异表达,并且由于唾液酸在与癌症发展和转移相关的生物功能中的不同参与而引起关注。在此,我们描述了使用 14P 血清消耗,随后使用窄 pH 范围酸性条带进行胶外等电聚焦,以在无标记液相色谱质谱(LC-MS)基于蛋白质组学分析之前简化和富集酸性蛋白质组和糖蛋白质组。所开发的平台能够检测到亚纳摩尔浓度的血清中存在的蛋白质,而使用各种生物信息学资源进行数据分析表明,许多检测到的蛋白质是组织渗漏蛋白或与特定细胞区室相关的蛋白质,而不是传统的分泌蛋白。与理论等电点(pI)值的比较还表明,一些检测到的蛋白质的 pI 值高于 IEF 步骤中应用的分离范围,这表明它们的存在可能是由于与蛋白质骨架连接的具有高唾液酸化程度的聚糖,以及其他翻译后修饰的存在。此类发现与在线 IEF 馏分的糖基化分析结果一致,在 pH 条从中性端向酸性端时,检测到糖链的唾液酸化程度逐渐增加。使用来自患有胃癌的患者的 pooled 血清应用该平台,包括在肿瘤切除手术前后,揭示了与细胞识别和细胞信号传导相关的许多差异表达蛋白。所开发的平台具有出色的灵敏度,并为聚焦于酸性蛋白质组的生物标志物发现研究中的应用提供了强大的潜力。