1. Traceless Immobilization of Analytes for High-Throughput Experiments with SAMDI Mass Spectrometry
- Author
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Milan Mrksich, Eric J. Berns, Kazi Y. Helal, and Azmain Alamgir
- Subjects
Molecular Structure ,Azirines ,Surface Properties ,010405 organic chemistry ,Chemistry ,General Chemistry ,Enzymes, Immobilized ,010402 general chemistry ,Mass spectrometry ,01 natural sciences ,Biochemistry ,Chemical reaction ,Combinatorial chemistry ,Catalysis ,High-Throughput Screening Assays ,0104 chemical sciences ,Adduct ,Matrix-assisted laser desorption/ionization ,Colloid and Surface Chemistry ,Cytochrome P-450 Enzyme System ,Covalent bond ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,Desorption ,Monolayer ,Molecule - Abstract
[Image: see text] Label-free assays, and particularly those based on the combination of mass spectroscopy with surface chemistries, enable high-throughput experiments of a broad range of reactions. However, these methods can still require the incorporation of functional groups that allow immobilization of reactants and products to surfaces prior to analysis. In this paper, we report a traceless method for attaching molecules to a self-assembled monolayer for matrix-assisted laser desorption and ionization (SAMDI) mass spectrometry. This method uses monolayers that are functionalized with a 3-trifluoromethyl-3-phenyl-diazirine group that liberates nitrogen when irradiated and gives a carbene that inserts into a wide range of bonds to covalently immobilize molecules. Analysis of the monolayer with SAMDI then reveals peaks for each of the adducts formed from molecules in the sample. This method is applied to characterize a P450 drug metabolizing enzyme and to monitor a Suzuki–Miyaura coupling chemical reaction and is important because modification of the substrates with a functional group would alter their activities. This method will be important for high-throughput experiments in many areas, including reaction discovery and optimization.
- Published
- 2018
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