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

被引:16
作者
Musso, Johana [1 ,2 ]
Buchmann, William [1 ,2 ]
Gonnet, Florence [1 ,2 ]
Jarroux, Nathalie [1 ,2 ]
Bellon, Sophie [3 ]
Frydman, Chiraz [3 ]
Brunet, Didier-Luc [3 ]
Daniel, Regis [1 ,2 ]
机构
[1] CNRS, Lab Anal & Modelisat Biol & Environm, UMR8587, F-91025 Evry, France
[2] Univ Evry Val DEssonne, Lab Anal & Modelisat Biol & Environm, F-91025 Evry, France
[3] Horiba Sci, F-91120 Palaiseau, France
关键词
SPR-MS; Biomolecular interaction analysis; Surface plasmon resonance; Mass spectrometry; Biological fluid; alpha-amylase; Lysozyme; BIOMOLECULAR INTERACTION ANALYSIS; NATIVE PROTEINS; IDENTIFICATION; BIA/MS; MS; COMBINATION; PROTEOMICS; FEMTOMOLE; CAPTURE; LIMIT;
D O I
10.1007/s00216-014-8373-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:1285 / 1294
页数:10
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