RationaleSurface-assisted laser desorption/ionization mass spectrometry (SALDI-MS) is an approach derived from matrix-assisted laser desorption/ionization (MALDI)-MS which overcomes the drawbacks associated with the use of organic matrices required to co-crystallize with the analytes. Indeed, nanomaterials commonly used in SALDI-MS as inert surfaces to promote desorption/ionization (D/I) ensure straightforward direct deposition of samples while providing mass spectra with ions only related to the compound of interest. The objective of this study was to develop a novel SALDI-MS approach based on steel plates that are surfaces very rapidly and easily tuned to perform the most efficient peptide detection as possible. To compare the SALDI efficacy of such metal substrates, D/I efficiency and deposit homogeneity were evaluated according to steel plate fabrication processes. MethodsThe studied surfaces were nanostructured steel plates that were chemically modified by perfluorosilane and textured according to different frequencies and laser writing powers. The capacity of each tested 100 surfaces was demonstrated by comparative analyses of a mixture of standard peptides (m/z 600-3000) performed with a MALDI-TOF instrument enabling MALDI, SALDI and imaging experiments. ResultsA peptide mix was used to screen the different surfaces depending on their D/I efficiency and their ability to ensure homogeneous deposit of the samples. For that purpose, deposition homogeneity was visualized owing to reconstructed ionic images from all protonated or sodiated ions of the 10 peptides constituting the standard mix. ConclusionsSeven surfaces were then selected satisfying the required D/I efficiency and deposit homogeneity criteria. Results obtained with these optimal surfaces were then compared with those recorded by MALDI-MS analyses used as references.
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Univ Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Coffinier, Yannick
Nguyen, Nhung
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Univ Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Univ Lille Nord France, IEMN, UMR 8520, CNRS, F-59652 Villeneuve Dascq, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Nguyen, Nhung
Drobecq, Herve
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Univ Lille Nord France, IBL, CNRS, UMR 8161, F-59021 Lille, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Drobecq, Herve
Melnyk, Oleg
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Univ Lille Nord France, IBL, CNRS, UMR 8161, F-59021 Lille, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Melnyk, Oleg
Thomy, Vincent
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Univ Lille Nord France, IEMN, UMR 8520, CNRS, F-59652 Villeneuve Dascq, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
Thomy, Vincent
Boukherroub, Rabah
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Univ Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, FranceUniv Lille Nord France, IRI, CNRS, USR 3078, F-59658 Villeneuve Dascq, France
机构:
Kansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, JapanKansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan
Arakawa, Ryuichi
Athanassiou, Evagelos K.
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Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Zurich, SwitzerlandKansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan
Athanassiou, Evagelos K.
Grass, Robert N.
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Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Zurich, SwitzerlandKansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan
Grass, Robert N.
Stark, Wendelin J.
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Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Zurich, SwitzerlandKansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan