Last data update: Nov 11, 2024. (Total: 48109 publications since 2009)
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Query Trace: Costin A [original query] |
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Characterization of N-terminal formaldehyde adducts to hemoglobin
Ospina M , Costin A , Barry AK , Vesper HW . Rapid Commun Mass Spectrom 2011 25 (8) 1043-50 A procedure to prepare and purify adducts of formaldehyde (FA) to the N-terminus of peptides was developed. FA-VHLTPEEK and FA-VLSPADK were produced with purities >95% upon incubation of the peptides with FA in phosphate-buffered saline (PBS) at a pH level of 7.4. The peptides were purified by preparative liquid chromatography and were characterized by their retention times in liquid chromatography, their fragmentation patterns obtained by tandem mass spectrometry, and their accurate mass and nuclear magnetic resonance measurements. This is the first time an imidazolidone-type structure has been reported for FA adducts. The same peptides were identified in tryptic digests of human hemoglobin incubated with FA at physiological conditions and in human hemoglobin specimens. These peptides are suitable for use as calibrators for the quantitative assessment of internal exposure to FA. Published in 2011 by John Wiley & Sons, Ltd. |
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