6533b82bfe1ef96bd128e3b2

RESEARCH PRODUCT

Shell palaeoproteomics: first application of peptide mass fingerprinting for the rapid identification of mollusc shells in archaeology.

Barbara PergolizziBeatrice DemarchiFrédéric MarinJorune SakalauskaiteJorune Sakalauskaite

subject

0301 basic medicineFreshwater bivalve[SHS.ARCHEO]Humanities and Social Sciences/Archaeology and PrehistoryBiophysicsShell (structure)BiologyBiochemistryPeptide Mapping03 medical and health sciencesPeptide mass fingerprintingAnimal Shells[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Mollusc shellMollusc shellAnimalsPeptide mass fingerprintPeptide-mass fingerprintPhylogenyShellomics030102 biochemistry & molecular biologyPhylogenetic treeMALDI-TOF mass spectrometry; Mollusc shell; Palaeoproteomics; Peptide mass fingerprint; ShellomicsMALDI-TOF mass spectrometryPalaeoproteomicsArchaeologyBivalvia030104 developmental biologyTaxonArchaeologyIdentification (biology)Peptides

description

10 pages; International audience; Molluscs were one of the most widely-used natural resources in the past, and their shells are abundant among archaeological findings. However, our knowledge of the variety of shells that were circulating in prehistoric times (and thus their socio-economic and cultural value) is scarce due to the difficulty of achieving taxonomic determination of fragmented and/or worked remains. This study aims to obtain molecular barcodes based on peptide mass fingerprints (PMFs) of intracrystalline proteins, in order to obtain shell identification. Palaeoproteomic applications on shells are challenging, due to low concentration of molluscan proteins and an incomplete understanding of their sequences. We explore different approaches for protein extraction from small-size samples (<20 mg), followed by MALDI-TOF-MS analysis. The SP3 (single-pot, solid-phase) sample preparation method was found to be the most successful in retrieving the intracrystalline protein fraction from seven molluscan shell taxa, which belong to different phylogenetic groups, possess distinct microstructures and are relevant for archaeology. Furthermore, all the shells analysed, including a 7000-year-old specimen of the freshwater bivalve Pseudunio, yielded good-quality distinctive spectra, demonstrating that PMFs can be used for shell taxon determination. Our work suggests good potential for large-scale screening of archaeological molluscan remains. SIGNIFICANCE: We characterise for the first time the peptide mass fingerprints of the intracrystalline shell protein fraction isolated from different molluscan taxa. We demonstrate that these proteins yield distinctive PMFs, even for shells that are phylogenetically related and/or that display similar microstructures. Furthermore, we extend the range of sample preparation approaches for "shellomics" by testing the SP3 method, which proved to be well-suited to shell protein extraction from small-size and protein-poor samples. This work thus lays the foundations for future large-scale applications for the identification of mollusc shells and other invertebrate remains from the archaeological and palaeontological records.

10.1016/j.jprot.2020.103920https://hal.archives-ouvertes.fr/hal-02969624/document