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Quo vadis blood protein adductomics?

Journal

ARCHIVES OF TOXICOLOGY
Volume 96, Issue 1, Pages 79-103

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00204-021-03165-2

Keywords

Biomonitoring; Albumin adducts; Hemoglobin adducts; Adductomics; Carcinogens

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Funding

  1. Projekt DEAL

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Chemicals are regularly measured in various settings, with biomonitoring in biological fluids serving as a tool to determine individual exposure. Different markers can be used for measuring both long-term and short-term exposure in the body. New approaches are needed to advance the field in the limitations of current methods.
Chemicals are measured regularly in air, food, the environment, and the workplace. Biomonitoring of chemicals in biological fluids is a tool to determine the individual exposure. Blood protein adducts of xenobiotics are a marker of both exposure and the biologically effective dose. Urinary metabolites and blood metabolites are short term exposure markers. Stable hemoglobin adducts are exposure markers of up to 120 days. Blood protein adducts are formed with many xenobiotics at different sites of the blood proteins. Newer methods apply the techniques developed in the field of proteomics. Larger adducted peptides with 20 amino acids are used for quantitation. Unfortunately, at present the methods do not reach the limits of detection obtained with the methods looking at single amino acid adducts or at chemically cleaved adducts. Therefore, to progress in the field new approaches are needed.

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