Fontenot J D, Ball J M, Miller M A, David C M, Montelaro R C
Louisiana State University.
Pept Res. 1991 Jan-Feb;4(1):19-25.
The routine production of peptides by manual or automated solid-phase synthesis protocols has gained widespread usage among a variety of biological scientists as new synthetic procedures have been introduced over the past several years. We report here a detailed analysis of Fmoc synthesis procedures to identify problematic reactions and to evaluate analytical procedures for monitoring the quality of peptides during and after synthesis. The results of these studies demonstrate double additions of particular amino acids during single coupling cycles, frequent incomplete deblocking of peptides by standard piperidine reactions, and the failure of the Kaiser ninhydrin test to detect free amino groups of certain amino acids at the N-terminus of synthetic peptides. These results suggest the need for more careful monitoring of Fmoc synthesis reactions than previously recognized or recommended in standard protocols. We demonstrate the utility of plasma desorption mass spectrometry (PDMS) in analyzing peptide products and recommend a minimum sequence of analytical quality control including HPLC and PDMS.
在过去几年中,随着新的合成方法的引入,通过手动或自动固相合成方案常规生产肽已在众多生物科学家当中得到广泛应用。我们在此报告对芴甲氧羰基(Fmoc)合成方法的详细分析,以识别有问题的反应,并评估在合成期间及合成后监测肽质量的分析方法。这些研究结果表明,在单个偶联循环中特定氨基酸会发生双加成,通过标准哌啶反应肽的脱保护常常不完全,并且凯氏茚三酮试验无法检测到合成肽N端某些氨基酸的游离氨基。这些结果表明,需要比标准方案中先前认识到的或推荐的更仔细地监测Fmoc合成反应。我们证明了等离子体解吸质谱(PDMS)在分析肽产物方面的实用性,并推荐了包括高效液相色谱(HPLC)和PDMS在内的最低限度的分析质量控制序列。