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• W2034115932 abstract "Combinatorial peptide libraries are a versatile tool for drug discovery. On-bead assays identify reactive peptides by enzyme-catalyzed staining and, usually, sequencing by Edman degradation. Unfortunately, the latter method is expensive and time-consuming and requires free N termini of the peptides. A method of rapid and unambiguous peptide sequencing by utilizing synthesis-implemented generation of termination sequences with subsequent matrix-assisted laser desorption ionization time of flight (MALDI-TOF) mass spectrometric analysis is introduced here. The required capped sequences are determined and optimized for a specific peptide library by a computer algorithm implemented in the program Biblio. A total of 99.7% of the sequences of a heptapeptide library sample could be decoded utilizing a single bead for each spectrum. To synthesize these libraries, an optimized capping approach has been introduced." @default.
• W2034115932 created "2016-06-24" @default.
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• W2034115932 date "2001-12-19" @default.
• W2034115932 modified "2023-10-03" @default.
• W2034115932 title "Mass Spectrometric Sequencing of Individual Peptides from Combinatorial Libraries via Specific Generation of Chain-Terminated Sequences" @default.
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• W2034115932 doi "https://doi.org/10.1021/cc010057x" @default.
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