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Protein sequences bound to mineral surfaces persist into deep time
Proteins persist longer in the fossil record than DNA, but the longevity, survival mechanisms and substrates remain contested. Here, we demonstrate the role of mineral binding in preserving the protein sequence in ostrich (Struthionidae) eggshell, including from thepalaeontological sites of Laetoli (3.8 Ma) and Olduvai Gorge (1.3 Ma) in Tanzania. By tracking protein diagenesis back in time we find consistent patterns of preservation, demonstrating authenticity of the surviving sequences. Molecular dynamics simulations of struthiocalcin-1 and -2, the dominant proteins within the eggshell, reveal that distinct domains bind to the mineral surface. It is the domain with the strongest calculated binding energy to the calcite surface that is selectively preserved. Thermal age calculations demonstrate that the Laetoli and Olduvai peptides are 50 times older than any previously authenticated sequence (equivalent to similar to 16 Ma at a constant 10 degrees C).
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File | Pages | Size | Access | |
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Publisher's official version | 50 | 2 Mo | ||
Supplementary file 1. Survival of ostrich eggshell proteins in time. The proteins identified in each ostrich eggshell sample are reported, together with the number of identified peptides | 32 | 781 Ko | ||
Supplementary file 2. Product ion spectra. Raw spectra (manually annotated on the basis of PEAKS assignments) of all the identified sequences identified in panel 1. 2–9: Copenhagen dataset; | 5 | 1 Mo | ||
Supplementary file 3. Diagenesis-induced modifications. Modifications detected in SCA-1 and SCA-2 sequences in all OES samples analysed. | 12 | 1 Mo | ||
Supplementary file 4. Full proteomics dataset. This Excel file reports all the peptide and protein data for ostrich eggshell samples and the blanks. | - | 6 Mo |