Sebela, M., Rašková, M., Nemethova, M., Weiss, V., & Marchetti-Deschmann, M. (2026). Protein Adducts Formed by Aldehyde Products of Spermine Oxidation. In 42nd IMMS Lisboa : Book of Abstracts (pp. 33–33).
E164-01-1 - Forschungsgruppe Massenspektrometrische Bio- und Polymeranalytik E056-04 - Fachbereich TU-DX: Towards Applications of 2D Materials E056-12 - Fachbereich ENROL DP E056-14 - Fachbereich Mature Tissue
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Published in:
42nd IMMS Lisboa : Book of Abstracts
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Date (published):
15-May-2026
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Event name:
42nd Informal Meeting on Mass Spectrometry (IMMS 2026)
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Event date:
13-May-2026 - 15-May-2026
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Event place:
Lissabon, Portugal
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Number of Pages:
1
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Keywords:
protein adducts; spermine; reactive aldehydes
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Abstract:
Polyamines including spermidine and spermine are positively charged molecules present in virtually all living
cells, where they function as key regulators of gene expression, cell growth and proliferation, apoptosis,
autophagy, and cellular stress responses [1]. Their metabolism involves tightly controlled synthesis from
ornithine (via putrescine) and S‑adenosylmethionine, which donates aminopropyl groups, together with
catabolic pathways mediated by amine oxidases. Polyamine degradation yields aminoaldehydes such as
spermine dialdehyde and 3‑aminopropanal, along with hydrogen peroxide. These aminoaldehydes can
release acrolein, a highly reactive protein‑modifying aldehyde [2].
To our knowledge, no mass‑spectrometry‑based study has directly characterized protein adducts formed by
spermine dialdehyde. We therefore attempted to generate this dialdehyde using pea seedling amine oxidase
incubated with spermine. MALDI‑MS showed that the expected dialdehyde had decomposed, as
3‑aminopropanal (m/z 74) was detected in the reaction mixture. Incubations of model peptides (e.g.,
angiotensin II and a tryptic bovine serum albumin digest) and proteins (e.g., β‑galactosidase and alcohol
dehydrogenase) with spermine in the presence of amine oxidase, or with the products formed during
spermine oxidation, yielded acrolein‑derived Schiff bases on lysine residues, Michael adducts on cysteine
residues, and additional amino‑acid modifications. The modification patterns closely matched those
generated by acrolein itself and by acrolein released from 3‑aminopropanal. We also observed protein
crosslinking, yielding covalent oligomers detectable by SDS‑PAGE and gel‑permeation chromatography.
Further characterization of these crosslinks is in progress.
REFERENCES
1. Schibalski, R.S. et al. (2024) Am. J. Physiol. Cell Physiol. 327, C341–C356.
2. Šebela, M. and Rašková, M. (2023) Molecules 28, 7429.
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Project title:
Veränderung von Proteinen durch reaktive Aldehyde aus dem Polyamin-Stoffwechsel: MULT 03/2025 (OeAD-GmbH - Agentur für Bildung und Internationalisierung)
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Research Areas:
Materials Characterization: 20% Biological and Bioactive Materials: 80%