Low-Invasive Sampling Method with Tape-Disc Sampling for the Taxonomic Identification of Archeological and Paleontological Bones by Proteomics
- Others:
- Miniaturisation pour la Synthèse, l'Analyse et la Protéomique - UAR 3290 (MSAP) ; Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)
- Culture et Environnements, Préhistoire, Antiquité, Moyen-Age (CEPAM) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UniCA)
- Histoire, Archéologie et Littérature des Mondes Anciens - UMR 8164 (HALMA) ; Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Ministère de la Culture (MC)
- Évolution, Écologie et Paléontologie (Evo-Eco-Paleo) - UMR 8198 (Evo-Eco-Paléo (EEP)) ; Université de Lille-Centre National de la Recherche Scientifique (CNRS)
- The authors acknowledge the IBiSA network for financial support of the UAR 3290 (MSAP) proteomics facility. The mass spectrometers were funded by University of Lille, CNRS, Région Hauts-de-France and the European Regional Development Fund. The authors deeply thank CNRS - Mission pour l'Interdisciplinarité for the funding of the Prot_HR_DAT project (2021-2022) and the AgroPastCN project (2020-2021). The authors are grateful to the Région Hauts-de-France for the funding of the ProtéOsHdF project (2021-2022) and the financial support from the IR INFRANALYTICS FR2054 CNRS for conducting the research is gratefully.
Description
Collagen from paleontological bones is an important organic material for isotopic measurement, radiocarbon and paleoproteomics analyzes, to provide information on diet, dating, taxonomy and phylogeny. Current paleoproteomics methods are destructive and require from a few milligrams to several tens of milligrams of bone for analysis. In many cultures, bones are raw materials for artefact which are conserved in museum which hampers to damage these precious objects during sampling. Here, we describe a low-invasive sampling method that identifies collagen, taxonomy and post-translational modifications from Holocene and Upper Pleistocene bones dated to 130,000 and 150 BC using dermatological skin tape-discs for sampling. The sampled bone micro-powders were digested following our highly optimized eFASP protocol, then analyzed by MALDI FTICR MS and LC-MS/MS for identifying the genus taxa of the bones. We show that this low-invasive sampling does not deteriorate the bones and achieves results similar to those obtained by more destructive sampling. Moreover, this sampling method can be carried out at archaeological sites or in museums.
Abstract
International audience
Additional details
- URL
- https://hal.science/hal-04660926
- URN
- urn:oai:HAL:hal-04660926v1
- Origin repository
- UNICA