Youngquist R S, Fuentes G R, Lacey M P, Keough T
Procter and Gamble Company, Miami Valley Laboratories, Cincinnati, Ohio 45239-8707.
Rapid Commun Mass Spectrom. 1994 Jan;8(1):77-81. doi: 10.1002/rcm.1290080115.
A termination synthesis approach has been developed to encode each resin bead in support-bound combinatorial peptide libraries with the information needed to establish the sequence of the full-length products also contained on the beads. Matrix-assisted laser desorption ionization mass spectrometry was then used to rapidly read the appropriate sequences. In addition to rapid peptide sequencing, the technique allows direct assessment of the quality of the synthetic library, since deletion peptides, side-reaction products and incomplete-deprotection products are readily observed. An anti-gp120 monoclonal antibody was screened against a hexapeptide library, and eight active peptides were isolated. Six of the eight peptides were shown to possess the exact recognition sequence for the antibody.
已开发出一种终止合成方法,用于在支持物结合的组合肽库中对每个树脂珠进行编码,该编码所需信息可用于确定珠子上所含全长产物的序列。然后使用基质辅助激光解吸电离质谱法快速读取相应序列。除了快速的肽测序外,该技术还能直接评估合成文库的质量,因为缺失肽、副反应产物和脱保护不完全产物都很容易被观察到。利用一个六肽库筛选了一种抗gp120单克隆抗体,分离出了8种活性肽。这8种肽中的6种被证明具有该抗体的确切识别序列。