Bone Proteomics Method Optimization for Forensic Investigations

Gent, Luke, Chiappetta, Maria Elena orcid iconORCID: 0009-0005-0458-671X, Hesketh, Stuart orcid iconORCID: 0000-0001-7855-2380, Palmowski, Pawel, Porter, Andrew, Bonicelli, Andrea orcid iconORCID: 0000-0002-9518-584X, Schwalbe, Edward C. and Procopio, Noemi orcid iconORCID: 0000-0002-7461-7586 (2024) Bone Proteomics Method Optimization for Forensic Investigations. Journal of Proteome Research . ISSN 1535-3893

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Official URL: https://doi.org/10.1021/acs.jproteome.4c00151

Abstract

The application of proteomic analysis to forensic skeletal remains has gained significant interest in improving biological and chronological estimations in medico-legal investigations. To enhance the applicability of these analyses to forensic casework, it is crucial to maximize throughput and proteome recovery while minimizing interoperator variability and laboratory-induced post-translational protein modifications (PTMs). This work compared different workflows for extracting, purifying, and analyzing bone proteins using liquid chromatography with tandem mass spectrometry (LC–MS)/MS including an in-StageTip protocol previously optimized for forensic applications and two protocols using novel suspension-trap technology (S-Trap) and different lysis solutions. This study also compared data-dependent acquisition (DDA) with data-independent acquisition (DIA). By testing all of the workflows on 30 human cortical tibiae samples, S-Trap workflows resulted in increased proteome recovery with both lysis solutions tested and in decreased levels of induced deamidations, and the DIA mode resulted in greater sensitivity and window of identification for the identification of lower-abundance proteins, especially when open-source software was utilized for data processing in both modes. The newly developed S-Trap protocol is, therefore, suitable for forensic bone proteomic workflows and, particularly when paired with DIA mode, can offer improved proteomic outcomes and increased reproducibility, showcasing its potential in forensic proteomics and contributing to achieving standardization in bone proteomic analyses for forensic applications.


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