Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States.
J Proteome Res. 2010 Dec 3;9(12):6091-100. doi: 10.1021/pr100904q. Epub 2010 Nov 11.
Although serum/plasma has been the preferred source for identification of disease biomarkers, these efforts have been met with little success, in large part due the relatively small number of highly abundant proteins that render the reliable detection of low abundant disease-related proteins challenging due to the expansive dynamic range of concentration of proteins in this sample. Proximal fluid, the fluid derived from the extracellular milieu of tissues, contains a large repertoire of shed and secreted proteins that are likely to be present at higher concentrations relative to plasma/serum. It is hypothesized that many, if not all, proximal fluid proteins exchange with peripheral circulation, which has provided significant motivation for utilizing proximal fluids as a primary sample source for protein biomarker discovery. The present review highlights recent advances in proximal fluid proteomics, including the various protocols utilized to harvest proximal fluids along with detailing the results from mass spectrometry- and antibody-based analyses.
虽然血清/血浆一直是鉴定疾病生物标志物的首选来源,但这些努力收效甚微,主要原因是相对较少的高度丰富的蛋白质,这使得可靠地检测低丰度与疾病相关的蛋白质具有挑战性,因为在这种样本中蛋白质的浓度具有广泛的动态范围。近体液是源自组织细胞外环境的液体,其中包含大量脱落和分泌的蛋白质,其浓度相对血浆/血清可能更高。据推测,许多(如果不是全部)近体液蛋白质与外周循环交换,这为利用近体液作为蛋白质生物标志物发现的主要样本来源提供了重要动力。本综述重点介绍了近体液蛋白质组学的最新进展,包括用于采集近体液的各种方案,以及详细介绍了基于质谱和抗体的分析结果。