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Proteomics as a new tool to study fingermark ageing in forensics
Fingermarks are trace evidence of great forensic importance, and their omnipresence makes them pivotal in crime investigation. Police and law enforcement authorities have exploited fingermarks primarily for personal identification, but crucial knowledge on when fingermarks were deposited is often la...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219553/ https://www.ncbi.nlm.nih.gov/pubmed/30401937 http://dx.doi.org/10.1038/s41598-018-34791-z |
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author | Oonk, Stijn Schuurmans, Tom Pabst, Martin de Smet, Louis C. P. M. de Puit, Marcel |
author_facet | Oonk, Stijn Schuurmans, Tom Pabst, Martin de Smet, Louis C. P. M. de Puit, Marcel |
author_sort | Oonk, Stijn |
collection | PubMed |
description | Fingermarks are trace evidence of great forensic importance, and their omnipresence makes them pivotal in crime investigation. Police and law enforcement authorities have exploited fingermarks primarily for personal identification, but crucial knowledge on when fingermarks were deposited is often lacking, thereby hindering crime reconstruction. Biomolecular constituents of fingermark residue, such as amino acids, lipids and proteins, may provide excellent means for fingermark age determination, however robust methodologies or detailed knowledge on molecular mechanisms in time are currently not available. Here, we address fingermark age assessment by: (i) drafting a first protein map of fingermark residue, (ii) differential studies of fresh and aged fingermarks and (iii), to mimic real-world scenarios, estimating the effects of donor contact with bodily fluids on the identification of potential age biomarkers. Using a high-resolution mass spectrometry-based proteomics approach, we drafted a characteristic fingermark proteome, of which five proteins were identified as promising candidates for fingermark age estimation. This study additionally demonstrates successful identification of both endogenous and contaminant proteins from donors that have been in contact with various bodily fluids. In summary, we introduce state-of-the-art proteomics as a sensitive tool to monitor fingermark aging on the protein level with sufficient selectivity to differentiate potential age markers from body fluid contaminants. |
format | Online Article Text |
id | pubmed-6219553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62195532018-11-07 Proteomics as a new tool to study fingermark ageing in forensics Oonk, Stijn Schuurmans, Tom Pabst, Martin de Smet, Louis C. P. M. de Puit, Marcel Sci Rep Article Fingermarks are trace evidence of great forensic importance, and their omnipresence makes them pivotal in crime investigation. Police and law enforcement authorities have exploited fingermarks primarily for personal identification, but crucial knowledge on when fingermarks were deposited is often lacking, thereby hindering crime reconstruction. Biomolecular constituents of fingermark residue, such as amino acids, lipids and proteins, may provide excellent means for fingermark age determination, however robust methodologies or detailed knowledge on molecular mechanisms in time are currently not available. Here, we address fingermark age assessment by: (i) drafting a first protein map of fingermark residue, (ii) differential studies of fresh and aged fingermarks and (iii), to mimic real-world scenarios, estimating the effects of donor contact with bodily fluids on the identification of potential age biomarkers. Using a high-resolution mass spectrometry-based proteomics approach, we drafted a characteristic fingermark proteome, of which five proteins were identified as promising candidates for fingermark age estimation. This study additionally demonstrates successful identification of both endogenous and contaminant proteins from donors that have been in contact with various bodily fluids. In summary, we introduce state-of-the-art proteomics as a sensitive tool to monitor fingermark aging on the protein level with sufficient selectivity to differentiate potential age markers from body fluid contaminants. Nature Publishing Group UK 2018-11-06 /pmc/articles/PMC6219553/ /pubmed/30401937 http://dx.doi.org/10.1038/s41598-018-34791-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Oonk, Stijn Schuurmans, Tom Pabst, Martin de Smet, Louis C. P. M. de Puit, Marcel Proteomics as a new tool to study fingermark ageing in forensics |
title | Proteomics as a new tool to study fingermark ageing in forensics |
title_full | Proteomics as a new tool to study fingermark ageing in forensics |
title_fullStr | Proteomics as a new tool to study fingermark ageing in forensics |
title_full_unstemmed | Proteomics as a new tool to study fingermark ageing in forensics |
title_short | Proteomics as a new tool to study fingermark ageing in forensics |
title_sort | proteomics as a new tool to study fingermark ageing in forensics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219553/ https://www.ncbi.nlm.nih.gov/pubmed/30401937 http://dx.doi.org/10.1038/s41598-018-34791-z |
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