TY - JOUR
T1 - Data-Independent Acquisition Mass Spectrometry as a Tool for Metaproteomics
T2 - Interlaboratory Comparison Using a Model Microbiome
AU - Rajczewski, Andrew T.
AU - Blakeley-Ruiz, J. Alfredo
AU - Meyer, Annaliese
AU - Vintila, Simina
AU - McIlvin, Matthew R.
AU - Van Den Bossche, Tim
AU - Searle, Brian C.
AU - Griffin, Timothy J.
AU - Saito, Mak A.
AU - Kleiner, Manuel
AU - Jagtap, Pratik D.
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/5
Y1 - 2025/5
N2 - Mass spectrometry (MS)-based metaproteomics is used to identify and quantify proteins in microbiome samples, with the frequently used methodology being data-dependent acquisition mass spectrometry (DDA-MS). However, DDA-MS is limited in its ability to reproducibly identify and quantify lower abundant peptides and proteins. To address DDA-MS deficiencies, proteomics researchers have started using Data-independent acquisition mass spectrometry (DIA-MS) for reproducible detection and quantification of peptides and proteins. We sought to evaluate the reproducibility and accuracy of DIA-MS metaproteomic measurements relative to DDA-MS using a mock community of known taxonomic composition. Artificial microbial communities of known composition were analyzed independently in three laboratories using DDA- and DIA-MS acquisition methods. In this study, DIA-MS yielded more protein and peptide identifications than DDA-MS in each laboratory for the particular instruments and software parameters chosen. In addition, the protein and peptide identifications were more reproducible in all laboratories and provided an accurate quantification of proteins and taxonomic groups in the samples. We also identified some limitations of current DIA tools when applied to metaproteomic data, highlighting specific needs to improve DIA tools enabling analysis of metaproteomic datasets from complex microbiomes. Ultimately, DIA-MS represents a promising strategy for MS-based metaproteomics due to its large number of detected proteins and peptides, reproducibility, deep sequencing capabilities, and accurate quantitation.
AB - Mass spectrometry (MS)-based metaproteomics is used to identify and quantify proteins in microbiome samples, with the frequently used methodology being data-dependent acquisition mass spectrometry (DDA-MS). However, DDA-MS is limited in its ability to reproducibly identify and quantify lower abundant peptides and proteins. To address DDA-MS deficiencies, proteomics researchers have started using Data-independent acquisition mass spectrometry (DIA-MS) for reproducible detection and quantification of peptides and proteins. We sought to evaluate the reproducibility and accuracy of DIA-MS metaproteomic measurements relative to DDA-MS using a mock community of known taxonomic composition. Artificial microbial communities of known composition were analyzed independently in three laboratories using DDA- and DIA-MS acquisition methods. In this study, DIA-MS yielded more protein and peptide identifications than DDA-MS in each laboratory for the particular instruments and software parameters chosen. In addition, the protein and peptide identifications were more reproducible in all laboratories and provided an accurate quantification of proteins and taxonomic groups in the samples. We also identified some limitations of current DIA tools when applied to metaproteomic data, highlighting specific needs to improve DIA tools enabling analysis of metaproteomic datasets from complex microbiomes. Ultimately, DIA-MS represents a promising strategy for MS-based metaproteomics due to its large number of detected proteins and peptides, reproducibility, deep sequencing capabilities, and accurate quantitation.
KW - artificial microbial community
KW - metaproteome
KW - microbiome
KW - microbiota
KW - synthetic community
UR - https://www.scopus.com/pages/publications/105002365438
UR - https://www.scopus.com/pages/publications/105002365438#tab=citedBy
U2 - 10.1002/pmic.202400187
DO - 10.1002/pmic.202400187
M3 - Article
C2 - 40211604
AN - SCOPUS:105002365438
SN - 1615-9853
VL - 25
JO - Proteomics
JF - Proteomics
IS - 9-10
M1 - e202400187
ER -