Pharmaceutical Sciences Faculty Publications
Identification of Membrane Proteins From Mammalian Cell/Tissue Using Methanol-Facilitated Solubilization and Tryptic Digestion Coupled with 2D-LC-MS/MS
Document Type
Article
Publication Date
1-1-2006
Journal Title
Nature Protocols
ISSN
1750-2799
Volume
1
Issue
6
First Page
2784
Last Page
2790
DOI
10.1038/nprot.2006.359
PubMed ID
17406535
Abstract
The core prerequisites for an efficient proteome-scale analysis of mammalian membrane proteins are effective isolation, solubilization, digestion and multidimensional liquid chromatography-tandem mass spectrometry (LC-MS/MS). This protocol is for analysis of the mammalian membrane proteome that relies on solubilization and tryptic digestion of membrane proteins in a buffer containing 60% (vol/vol) methanol. Tryptic digestion is followed by strong cation exchange (SCX) chromatography and reversed phase (RP) chromatography coupled online with MS/MS for protein identification. The use of a methanol-based buffer eliminates the need for reagents that interfere with chromatographic resolution and ionization of the peptides (e.g., detergents, chaotropes, inorganic salts). Sample losses are minimized because solubilization and digestion are carried out in a single tube avoiding any sample transfer or buffer exchange between these steps. This protocol is compatible with stable isotope labeling at the protein and peptide level, enabling identification and quantitation of integral membrane proteins. The entire procedure--beginning with isolated membrane fraction and finishing with MS data acquisition--takes 4-5 d.
Keywords
Chromatography, liquid, membrane proteins, proteomics, solubility, tandem mass spectrometry, trypsin
Recommended Citation
Blonder, Josip; Chan, King C.; Issaq, Haleem J.; and Veenstra, Timothy D., "Identification of Membrane Proteins From Mammalian Cell/Tissue Using Methanol-Facilitated Solubilization and Tryptic Digestion Coupled with 2D-LC-MS/MS" (2006). Pharmaceutical Sciences Faculty Publications. 381.
https://digitalcommons.cedarville.edu/pharmaceutical_sciences_publications/381