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Mass spectrometry-based proteomic strategy for ecchymotic skin examination in forensic pathology.

Authors :
Toma L
Vignali G
Maffioli E
Tambuzzi S
Giaccari R
Mattarozzi M
Nonnis S
Milioli M
Franceschetti L
Paredi G
Negri A
Riccardi B
Cattaneo C
Careri M
Tedeschi G
Bruno S
Source :
Scientific reports [Sci Rep] 2023 Apr 14; Vol. 13 (1), pp. 6116. Date of Electronic Publication: 2023 Apr 14.
Publication Year :
2023

Abstract

Mass spectrometry (MS)-based proteomics has recently attracted the attention from forensic pathologists. This work is the first report of the development of a shotgun bottom-up proteomic approach based on rapid protein extraction and nano-liquid chromatography/high-resolution mass spectrometry applied to full-thickness human skin for the differential analysis of normal and ecchymotic tissues to identify new biomarkers for bruise characterization and dating. We identified around 2000 proteins from each pooled extract. The method showed excellent precision on independent replicates, with Pearson correlation coefficients always higher than 95%. Glycophorin A, a known biomarker of vital wounds from immunochemical studies, was identified only in ecchymotic tissues, as confirmed by Western blotting analysis. This finding suggests that this protein can be used as a MS-detectable biomarker of wound vitality. By focusing on skin samples from individuals with known wound dating, besides Glycophorin A, other proteins differentially expressed in ecchymotic samples and dependant on wound age were identified, although further analysis on larger datasets are needed to validate these findings. This study paves the way for an in-depth investigation of the potential of MS-based techniques for wound examination in forensic pathology, overcoming the limitations of immunochemical assays.<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
2045-2322
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
37059833
Full Text :
https://doi.org/10.1038/s41598-023-32520-9