4.7 Article

SubCellBarCode: integrated workflow for robust spatial proteomics by mass spectrometry

Journal

NATURE PROTOCOLS
Volume 17, Issue 8, Pages 1832-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41596-022-00699-2

Keywords

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Funding

  1. Swedish Foundation for Strategic Research
  2. Swedish Cancer Society
  3. Swedish Research Council
  4. Swedish Childhood Cancer Foundation
  5. Cancer Research Funds of Radiumhemmet
  6. Stockholm's County Council (ALF funding)

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The subcellular localization of a protein is crucial for understanding its functions. In this study, a mass spectrometry- and bioinformatics-based pipeline was developed to generate a comprehensive resource for protein subcellular localization in multiple human cancer cell lines. The protocol includes a detailed wet-lab procedure, quantitative MS-data analysis, machine learning-based classification, and visualization of the output. The pipeline was evaluated using different peptide pre-fractionation approaches and proved to be straightforward and robust, with the entire process being completed within 1-2 weeks.
The molecular functions of a protein are defined by its inherent properties in relation to its environment and interaction network. Within a cell, this environment and network are defined by the subcellular location of the protein. Consequently, it is crucial to know the localization of a protein to fully understand its functions. Recently, we have developed a mass spectrometry- (MS) and bioinformatics-based pipeline to generate a proteome-wide resource for protein subcellular localization across multiple human cancer cell lines (www.subcellbarcode.org ). Here, we present a detailed wet-lab protocol spanning from subcellular fractionation to MS-sample preparation and analysis. A key feature of this protocol is that it includes all generated cell fractions without discarding any material during the fractionation process. We also describe the subsequent quantitative MS-data analysis, machine learning-based classification, differential localization analysis and visualization of the output. For broad applicability, we evaluated the pipeline by using MS data generated by two different peptide pre-fractionation approaches, namely high-resolution isoelectric focusing and high-pH reverse-phase fractionation, as well as direct analysis without pre-fractionation by using long-gradient liquid chromatography-MS. Moreover, an R package covering the dry-lab part of the method was developed and made available through Bioconductor. The method is straightforward and robust, and the entire protocol, from cell harvest to classification output, can be performed within 1-2 weeks. The protocol enables accurate classification of proteins to 15 compartments and 4 neighborhoods, visualization of the output data and differential localization analysis including treatment-induced protein relocalization, condition-dependent localization or cell type-specific localization. The SubCellBarCode package is freely available at https://bioconductor.org/packagesidevelibioc/html/SubCellEarCode.html.

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