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Updated: Apr 30, 2026
In situ Subcellular Fractionation of Adherent and Non-adherent Mammalian Cells
Published on: July 23, 2010
Determining protein subcellular localization in mammalian cell culture with biochemical fractionation and iTRAQ
Andy Christoforou1, Alfonso Martinez Arias, Kathryn S Lilley
1Department of Genetics, University of Cambridge, Downing Street, Cambridge, CB2 3EH, UK, ac587@cam.ac.uk.
Abstract:
Protein subcellular localization is a fundamental feature of posttranslational functional regulation. Traditional microscopy based approaches to study protein localization are typically of limited throughput, and dependent on the availability of antibodies with high specificity and sensitivity, or fluorescent fusion proteins. In this chapter we describe how Localization of Organelle Proteins by Isotope Tagging (LOPIT), a mass spectrometry based workflow coupling biochemical fractionation and iTRAQ™ 8-plex quantification, can be applied for the high-throughput characterization of protein localization in a mammalian cell culture line.
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