Your browser doesn't support javascript.
loading
Bone Proteomics Method Optimization for Forensic Investigations.
Gent, Luke; Chiappetta, Maria Elena; Hesketh, Stuart; Palmowski, Pawel; Porter, Andrew; Bonicelli, Andrea; Schwalbe, Edward C; Procopio, Noemi.
Afiliação
  • Gent L; School of Law and Policing, Research Centre for Field Archaeology and Forensic Taphonomy, University of Central Lancashire, Preston PR1 2HE, United Kingdom.
  • Chiappetta ME; School of Law and Policing, Research Centre for Field Archaeology and Forensic Taphonomy, University of Central Lancashire, Preston PR1 2HE, United Kingdom.
  • Hesketh S; Department of Biology, Ecology and Earth Sciences (DiBEST), University of Calabria, Arcavacata di Rende 87036, Italy.
  • Palmowski P; School of Medicine, University of Central Lancashire, Preston PR1 2HE, United Kingdom.
  • Porter A; NUPPA Facility, Medical School, Newcastle University, Newcastle Upon Tyne NE1 7RU, United Kingdom.
  • Bonicelli A; NUPPA Facility, Medical School, Newcastle University, Newcastle Upon Tyne NE1 7RU, United Kingdom.
  • Schwalbe EC; School of Law and Policing, Research Centre for Field Archaeology and Forensic Taphonomy, University of Central Lancashire, Preston PR1 2HE, United Kingdom.
  • Procopio N; Department of Applied Sciences, Northumbria University, Newcastle Upon Tyne NE1 8ST, United Kingdom.
J Proteome Res ; 23(5): 1844-1858, 2024 May 03.
Article em En | MEDLINE | ID: mdl-38621258
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.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Espectrometria de Massas em Tandem Limite: Humans Idioma: En Revista: J Proteome Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Espectrometria de Massas em Tandem Limite: Humans Idioma: En Revista: J Proteome Res Ano de publicação: 2024 Tipo de documento: Article