Results from a multi-laboratory ocean metaproteomic intercomparison: effects of LC-MS acquisition and data analysis procedures

Autor: M. A. Saito, J. K. Saunders, M. R. McIlvin, E. M. Bertrand, J. A. Breier, M. M. Brisbin, S. M. Colston, J. R. Compton, T. J. Griffin, W. J. Hervey, R. L. Hettich, P. D. Jagtap, M. Janech, R. Johnson, R. Keil, H. Kleikamp, D. Leary, L. Martens, J. S. P. McCain, E. Moore, S. Mehta, D. M. Moran, J. Neibauer, B. A. Neely, M. V. Jakuba, J. Johnson, M. Duffy, G. J. Herndl, R. Giannone, R. Mueller, B. L. Nunn, M. Pabst, S. Peters, A. Rajczewski, E. Rowland, B. Searle, T. Van Den Bossche, G. J. Vora, J. R. Waldbauer, H. Zheng, Z. Zhao
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Biogeosciences, Vol 21, Pp 4889-4908 (2024)
Druh dokumentu: article
ISSN: 1726-4170
1726-4189
DOI: 10.5194/bg-21-4889-2024
Popis: Metaproteomics is an increasingly popular methodology that provides information regarding the metabolic functions of specific microbial taxa and has potential for contributing to ocean ecology and biogeochemical studies. A blinded multi-laboratory intercomparison was conducted to assess comparability and reproducibility of taxonomic and functional results and their sensitivity to methodological variables. Euphotic zone samples from the Bermuda Atlantic Time-series Study (BATS) in the North Atlantic Ocean collected by in situ pumps and the autonomous underwater vehicle (AUV) Clio were distributed with a paired metagenome, and one-dimensional (1D) liquid chromatographic data-dependent acquisition mass spectrometry analysis was stipulated. Analysis of mass spectra from seven laboratories through a common bioinformatic pipeline identified a shared set of 1056 proteins from 1395 shared peptide constituents. Quantitative analyses showed good reproducibility: pairwise regressions of spectral counts between laboratories yielded R2 values averaged 0.62±0.11, and a Sørensen similarity analysis of the top 1000 proteins revealed 70 %–80 % similarity between laboratory groups. Taxonomic and functional assignments showed good coherence between technical replicates and different laboratories. A bioinformatic intercomparison study, involving 10 laboratories using eight software packages, successfully identified thousands of peptides within the complex metaproteomic datasets, demonstrating the utility of these software tools for ocean metaproteomic research. Lessons learned and potential improvements in methods were described. Future efforts could examine reproducibility in deeper metaproteomes, examine accuracy in targeted absolute quantitation analyses, and develop standards for data output formats to improve data interoperability. Together, these results demonstrate the reproducibility of metaproteomic analyses and their suitability for microbial oceanography research, including integration into global-scale ocean surveys and ocean biogeochemical models.
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