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Carboxy-terminal degradation of peptides using perfluoroacyl anhydrides. A C-terminal sequencing method.

European journal of biochemistry (1995-03-01)
K Takamoto, M Kamo, K Kubota, K Satake, A Tsugita
RESUMEN

An accurate carboxy-terminal sequencing method has long been sought to complement the Edman degradation procedure for amino-terminal amino acid sequence analysis. The method presented here is a unique and simple method to partly fulfill the needs. Exposure of a polypeptide to perfluoroacyl anhydride vapor at -20 degrees C for 0.5-1 h causes sequential chemical degradation of the molecule from the C-terminus. Fast-atom-bombardment mass spectrometric analysis of the resultant mixture of C-terminally truncated molecules permits the determination of the C-terminal sequence by simple calculation of the mass differences in molecular ions. Experiments suggested that this C-terminal degradation proceeds by active intermediates such as oxazolone at the C-terminal carboxyl residues.

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Sigma-Aldrich
Pentafluoropropionic anhydride, purum, ≥97.0% (GC)
Supelco
Pentafluoropropionic anhydride, for GC derivatization, LiChropur, 99%