Abstract
We describe a method, filter-aided sample preparation (FASP), which combines the advantages of in-gel and in-solution digestion for mass spectrometry–based proteomics. We completely solubilized the proteome in sodium dodecyl sulfate, which we then exchanged by urea on a standard filtration device. Peptides eluted after digestion on the filter were pure, allowing single-run analyses of organelles and an unprecedented depth of proteome coverage.
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Acknowledgements
We thank S. Ren for bioinformatic support. This work was supported by the Max Planck Society for the Advancement of Science, High-throughput Epigenetic Regulatory Organization In Chromatin (HEROIC), Role of Ubiquitin and Ubiquitin-like Modifiers in Cellular Regulation (RUBICON) 6th Framework grants of the European Commission and the Munich Center for Integrated Protein Science (CIPSM).
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Supplementary Text and Figures
Supplementary Figures 1–11, Supplementary Tables 1–4, Supplementary Protocol (PDF 1745 kb)
Supplementary Data 1
Analysis of total lysates of Hela cells (XLS 6405 kb)
Supplementary Data 2
Analysis of total lysates of Hela cells fractionated by IEF. (XLS 8640 kb)
Supplementary Data 3
Analysis of total lysates of a mouse brain. (XLS 2253 kb)
Supplementary Data 4
Analysis of total lysate of mouse liver. (XLS 3026 kb)
Supplementary Data 5
Analysis of total lysates of Hela cells digested with different endoproteinases. (XLS 10876 kb)
Supplementary Data 6
Analysis of total lysates of Hela cells digested under different conditions. (XLS 6731 kb)
Supplementary Data 7
Analysis of total lysates of mitochondria isolated from mouse liver. (XLS 236 kb)
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Wiśniewski, J., Zougman, A., Nagaraj, N. et al. Universal sample preparation method for proteome analysis. Nat Methods 6, 359–362 (2009). https://doi.org/10.1038/nmeth.1322
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DOI: https://doi.org/10.1038/nmeth.1322