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在人类血浆中进行免疫-MALDI-MS 和芯片上的生物标志物特征分析,达到飞摩尔水平。

Immuno-MALDI-MS in human plasma and on-chip biomarker characterizations at the femtomole level.

机构信息

Institut FEMTO-ST, Université de Franche Comté, CLIPP (Clinical-Innovation Proteomic Platform), 25044 Besançon, France.

出版信息

Sensors (Basel). 2012 Nov 6;12(11):15119-32. doi: 10.3390/s121115119.

Abstract

Immuno-SPR-MS is the combination of immuno-sensors in biochip format with mass spectrometry. This association of instrumentation allows the detection and the quantification of proteins of interest by SPR and their molecular characterization by additional MS analysis. However, two major bottlenecks must be overcome for a wide diffusion of the SPR-MS analytical platform: (i) To warrant all the potentialities of MS, an enzymatic digestion step must be developed taking into account the spot formats on the biochip and (ii) the biological relevancy of such an analytical solution requires that biosensing must be performed in complex media. In this study, we developed a procedure for the detection and the characterization at ~1 µg/mL of the LAG3 protein spiked in human plasma. The analytical performances of this new method was established, particularly its specificity (S/N > 9) and sensitivity (100% of LAG3 identification with high significant mascot score >68 at the femtomole level). The collective and automated on-chip MALDI-MS imaging and analysis based on peptidic fragments opens numerous applications in the fields of proteomics and diagnosis.

摘要

免疫 SPR-MS 是将生物芯片格式的免疫传感器与质谱结合在一起。这种仪器的组合允许通过 SPR 检测和定量感兴趣的蛋白质,并通过额外的 MS 分析对其进行分子表征。然而,要广泛推广 SPR-MS 分析平台,必须克服两个主要的瓶颈:(i) 为了保证 MS 的所有潜力,必须开发一种酶解步骤,同时考虑到生物芯片上的斑点格式;(ii) 这种分析解决方案的生物学相关性要求生物传感必须在复杂的介质中进行。在本研究中,我们开发了一种在人血浆中检测和表征浓度为 ~1 µg/mL 的 LAG3 蛋白的方法。该新方法的分析性能得到了确立,特别是其特异性(S/N > 9)和灵敏度(在飞摩尔水平下,高显著 Mascot 评分 >68 可实现 100%的 LAG3 鉴定)。基于肽片段的集体和自动化芯片上 MALDI-MS 成像和分析为蛋白质组学和诊断领域开辟了许多应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ef2/3522956/805d848e8f65/sensors-12-15119u1.jpg

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