
The identification and characterization of biotinylated lysyl residues in a polypeptide chain by automated sequence analysis is described. An in depth analytical study was conducted for the delineation of N epsilon modification of lysyl residues with N-hydroxysuccinimide esters of biotin and 6-aminohexanoic biotin. Confirmation of the structure of the phenylthiohydantoin derivatives of N epsilon biotinylated lysine was achieved by mass spectrometry. The analytical study focused on the identification of biotinylated lysine-4 of neuropeptide Y which served as a model peptide for the analytical procedures detailed.
Lysine, Molecular Sequence Data, Biotin, Proteins, Chemistry Techniques, Analytical, Phenylthiohydantoin, Humans, Neuropeptide Y, Amino Acid Sequence, Peptides, Chromatography, High Pressure Liquid
Lysine, Molecular Sequence Data, Biotin, Proteins, Chemistry Techniques, Analytical, Phenylthiohydantoin, Humans, Neuropeptide Y, Amino Acid Sequence, Peptides, Chromatography, High Pressure Liquid
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