Tissue subcellular fractionation and protein extraction for use in mass-spectrometry-based proteomics
Abstract
We have shown that sample fractionation is an effective method for increasing the detection coverage of the proteome of complex samples, such as organs, by mass-spectrometric techniques. Further fractionating a sample based on subcellular compartments can generate molecular information on the state of a tissue and the distribution of its protein components. Although many methods exist for fractionating proteins, the method described here can capture the majority of subcellular fractions simultaneously at reasonable purity. The scalability of this method makes it amenable to small samples, such as embryonic tissues, in addition to larger tissues. The protocol described is for the general fractionation and extraction of proteins from organs or tissues for subsequent analysis by mass spectrometry. It uses differential centrifugation in density gradients to isolate nuclear, cytosolic, mitochondrial and mixed microsomal (Golgi, endoplasmic reticulum, other vesicles and plasma membrane) fractions. Once the fractions are isolated, they are extracted for protein and the samples can then be frozen for processing and analysis at a later date. The procedure can typically be completed in 5 h.
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Purification of proteins from distinct subcellular compartments allows separate assay of proteins in the nucleus, cytosol, cytoskeleton, endoplasmic reticulum, and plasma membrane.
“The various methods available for spectra acquisition and quantification can be complemented by purification of protein from distinct sub-cellular compartments, which allows investigators to specifically and separately assay proteins located in the nucleus, cytosol, cytoskeleton, endoplasmic reticulum, and plasma membrane31.”
From Decoding neuroproteomics: integrating the genome, translatome and functional anatomy (2014) · cites this paper as [31]
Density/gradient centrifugation can purify sub-cellular fractions such as plasma membrane, lipid rafts, mitochondria, or Golgi, offering sub-cellular resolution.
“The application of density/gradient centrifugation for purification of other sub-cellular fractions such as the plasma membrane or lipid rafts, or of specific types of organelles like mitochondria of the Golgi, offers sub-cellular resolution31”
From Decoding neuroproteomics: integrating the genome, translatome and functional anatomy (2014) · cites this paper as [31]
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References 11 · Cited by 352
- Authors
- Cox, B., & Emili, A.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Cox, Brian
- Venue
- Nature Protocols
- Published
- 2006-11
- Volume
- 1
- Issue
- 4
- Pages
- 1872-1878
- ISSN
- 1750-2799 (ISSN-L)
- 1754-2189
- OpenAlex
- W2039231543
- Cited by
- 352
- References
- 11
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 20 · 2023: 10 · 2022: 8 · 2021: 21 · 2020: 17 · 2019: 28 · 2018: 26 · 2017: 28 · 2016: 23 · 2015: 26 · 2014: 18 · 2013: 17 · 2012: 23
- FWCI
- 3.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Protocols (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Council
- Canadian Institutes of Health Research
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Physical Sciences › Chemistry › Spectroscopy › Mass Spectrometry Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- subcellular fractionation, tissue proteomics, protein extraction, differential centrifugation, density gradient fractionation, nuclear fraction, cytosolic fraction, mitochondrial fraction, microsomal fraction, embryonic tissue, proteome coverage
- MeSH terms
- Cell Fractionation, Proteins, Mass Spectrometry, Proteomics
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