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Electrochemically initiated tagging of thiols using an electrospray ionization based liquid microjunction surface sampling probe two‐electrode cell
Author(s) -
Van Berkel Gary J.,
Kertesz Vilmos
Publication year - 2009
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.4014
Subject(s) - chemistry , hydroquinone , electrode , analyte , analytical chemistry (journal) , electrochemistry , electrospray ionization , chromatography , mass spectrometry , organic chemistry
Abstract This paper reports on the conversion of a liquid microjunction surface sampling probe (LMJ‐SSP) into a two‐electrode electrochemical cell using a conductive sample surface and the probe as the two electrodes with an appropriate battery powered circuit. With this LMJ‐SSP, two‐electrode cell arrangement, tagging of analyte thiol functionalities (in this case peptide cysteine residues) with hydroquinone tags was initiated electrochemically using a hydroquinone‐doped solution when the analyte either was initially in solution or was sampled from a surface. Efficient tagging (∼90%), at flow rates of 5–10 µL/min, could be achieved for up to at least two cysteines on a peptide. The high tagging efficiency observed was explained with a simple kinetic model. In general, the incorporation of a two‐electrode electrochemical cell, or other multiple electrode arrangement, into the LMJ‐SSP is expected to add to the versatility of this approach for surface sampling and ionization coupled with mass spectrometric detection. Published in 2009 by John Wiley & Sons, Ltd.