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S ‐Pyridylethylation of intact polyacrylamide gels and in situ digestion of electrophoretically separated proteins: A rapid mass spectrometric method for identifying cysteine‐containing peptides
Author(s) -
Moritz Robert L.,
Eddes James S.,
Reid Gavin E.,
Simpson Richard J.
Publication year - 1996
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.1150170512
Subject(s) - chromatography , chemistry , peptide , trypsin , peptide mass fingerprinting , edman degradation , bottom up proteomics , cysteine , mass spectrometry , tandem mass spectrometry , gel electrophoresis , coomassie brilliant blue , polyacrylamide gel electrophoresis , electrospray , digestion (alchemy) , sample preparation in mass spectrometry , biochemistry , protein mass spectrometry , electrospray ionization , peptide sequence , proteomics , staining , enzyme , biology , genetics , gene
In‐gel proteolytic digestion of acrylamide‐gel separated proteins is a method widely used for generating peptide fragments for the purpose of identifying proteins by Edman degratation, tandem mass spectrometry, and peptide‐mass fingerprinting. However, it is well recognised for disulfide‐bonded proteins electrophoresed under reducing conditions that if no precautions are taken to minimise disulfide bond formation during protein digestion or peptide isolation, complex peptide maps can result. Here, we describe an improved method for in‐gel protein digestion. It consists of first reducing and S ‐pyridylethylating Coomassie Brilliant Blue R‐250‐stained proteins immobilised in the whole gel slab with dithiothreitol and 4‐vinylpyridine, excising the individual stained and alkylated proteins, and then digesting them in situ in the gel matrix with trypsin or Achromobacter lyticus protease I. Peptide fragments generated in this manner are extracted from the gel piece and purified to homogeneity by a rapid (≤12 min) reversed‐phase high performance liquid chromatography (HPLC) procedure, based upon conventional silica supports. Recoveries of peptides are increased by S ‐pyridylethylation of acrylamide‐immbilised proteins prior to in‐gel digestion. Further, the levels of gel‐related contaminants, which otherwise result in suppression of sample signals during electrosprayionisation mass spectrometry, are greatly reduced by the reduction / alkylation step. Additionally, we demonstrate that S ‐β‐(4‐pyridylethyl)‐cysteine containing peptides can be readily identified during reversed‐phase HPLC by absorance at 254 nm, and during electrospray ionisation tandem mass spectrometry by the appearance of a characteristic‐pyridylethyl fragment ion of 106 Da. The position of cysteine residues in a sequence can be determined as phenylthiohydantoin S ‐β‐(4‐pyridylethyl)‐cysteine during Edman degradation, and by tandem mass spectrometry.