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Biomarkers probed in saliva by surface plasmon resonance imaging coupled to matrix-assisted laser desorption/ionization mass spectrometry in array format

机译:通过表面等离子体共振成像与基质辅助激光解吸/电离质谱联用阵列形式在唾液中探测的生物标志物

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摘要

Detection of protein biomarkers is of major interest in proteomics. This work reports the analysis of protein biomarkers directly from a biological fluid, human saliva, by surface plasmon resonance imaging coupled to mass spectrometry (SPRi-MS), using a functionalized biochip in an array format enabling multiplex SPR-MS analysis. The SPR biochip presented a gold surface functionalized by a self-assembled monolayer of short poly(ethylene oxide) chains carrying an N-hydroxysuccinimide end-group for the immobilization of antibodies. The experiments were accomplished without any sample pre-purification or spiking with the targeted biomarkers. SPRi monitoring of the interactions, immune capture from the biochip surface, and finally onchip matrix-assisted laser desorption/ionization-MS structural identification of two protein biomarkers, salivary alpha-amylase and lysozyme, were successively achieved directly from saliva at the femtomole level. For lysozyme, the on-chip MS identification was completed by a proteomic analysis based on an on-chip proteolysis procedure and a peptide mass fingerprint.
机译:蛋白质生物标志物的检测是蛋白质组学的主要兴趣。这项工作报告了使用功能化生物芯片以阵列格式进行多重SPR-MS分析,通过表面等离振子共振成像与质谱(SPRi-MS)耦合,直接从生物流体,人唾液中分析蛋白质生物标志物。 SPR生物芯片展示了一个金表面,该表面被带有聚N-羟基琥珀酰亚胺末端基团的短聚环氧乙烷短链的自组装单层功能化,从而固定了抗体。无需任何样品预纯化或添加目标生物标志物即可完成实验。 SPRi的相互作用监测,从生物芯片表面的免疫捕获以及最后在芯片上的唾液α-淀粉酶和溶菌酶两个蛋白质生物标记的芯片上基质辅助激光解吸/电离-MS结构鉴定,都是直接从唾液中获得的。对于溶菌酶,基于芯片上蛋白水解程序和肽质量指纹图谱的蛋白质组分析完成了芯片上MS鉴定。

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