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Characterization of N-terminal formaldehyde adducts to hemoglobin

Authors

  • Maria Ospina,

    Corresponding author
    • Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, USA
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  • Alina Costin,

  • Adrienne K. Barry,

  • Hubert W. Vesper


  • This article is a U.S. Government work and is in the public domain in the U.S.A.

M. Ospina, CDC, 4770 Buford Highway, MS-F25, Atlanta, GA 30341, USA

E-mail: MOspina@cdc.gov

Abstract

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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