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Multiwell in‐gel protein digestion and microscale sample preparation for protein identification by mass spectrometry
Author(s) -
Pluskal Malcolm G.,
Bogdanova Alla,
Lopez Mary,
Gutierrez Sara,
Pitt Aldo M.
Publication year - 2002
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/1615-9861(200202)2:2<145::aid-prot145>3.0.co;2-y
Subject(s) - microscale chemistry , mass spectrometry , chromatography , digestion (alchemy) , sample preparation , chemistry , bottom up proteomics , proteomics , sample preparation in mass spectrometry , protein mass spectrometry , tandem mass spectrometry , biochemistry , electrospray ionization , mathematics education , mathematics , gene
In‐gel peptide digestion has become a widely used technique for characterizing proteins resolved by two‐dimensional gel electrophoresis. Peptides generated from gel pieces are frequently contaminated with detergent and salts. Prior to matrix‐assisted laser desorption/ionization‐time of flight mass spectrometry analysis, these contaminants are removed using micro scale C18 sample preparation columns. In this paper, data are presented to demonstrate the application of a solvent resistant MultiScreen 96‐well plate with a low peptide binding membrane and ZipTip® micropipette based sample preparation. Recoveries of peptides ( m/z of 1000 to 5000 Da) derived from standard protein protease digests, were estimated at various stages of the analytical process. An optimized protocol has been established and all the reagents and consumables have been packaged in a ready to use commercial kit. Data will be presented to show the application of this technology package to accelerate the throughput of protein characterization by protease fragmentation.