Chiu Chi-Li, Randall Sarah, Molloy Mark P
Department of Chemistry & Biomolecular Sciences and Australian Proteome Analysis Facility, Macquarie University, Sydney 2109, Australia.
Bioanalysis. 2009 Jul;1(4):847-55. doi: 10.4155/bio.09.56.
The plasma proteome offers a wealth of opportunity to develop protein-based assays for diagnostic, prognostic and predictive biomarkers. Nonetheless, the unique properties of plasma, with its high dynamic range of protein concentrations and the vast complexity of protein species, present considerable analytical challenges. The continuing maturation of proteomic technologies, in particular biological MS instrumentation and immunoaffinity sample preparation strategies, is driving progress in the field. Selected reaction monitoring (SRM)-MS of peptides derived from plasma proteins is one such development that facilitates high-fidelity selection and quantitation with only minimal prior sample enrichment, while coupling targeted immunoaffinity enrichment prior to SRM-MS further enhances detection of less-abundant plasma proteins present in the subnanogram per millilitre concentration. This article reviews recent progress in the bioanalysis of plasma proteins driven by SRM-MS.
血浆蛋白质组为开发基于蛋白质的诊断、预后和预测生物标志物检测方法提供了丰富的机会。然而,血浆具有独特的性质,其蛋白质浓度动态范围高且蛋白质种类极其复杂,这带来了相当大的分析挑战。蛋白质组学技术的不断成熟,尤其是生物质谱仪器和免疫亲和样品制备策略,正在推动该领域的进展。对源自血浆蛋白的肽段进行选择反应监测(SRM)-质谱分析就是这样一种进展,它只需极少的预先样品富集就能实现高保真选择和定量,而在SRM-质谱分析之前结合靶向免疫亲和富集则进一步增强了对每毫升浓度低于纳克的低丰度血浆蛋白的检测。本文综述了由SRM-质谱分析推动的血浆蛋白生物分析的最新进展。