Brauer A W, Oman C L, Margolies M N
Anal Biochem. 1984 Feb;137(1):134-42. doi: 10.1016/0003-2697(84)90359-2.
Background generated during the cleavage step of the Edman degradation is a major obstacle to extended automated amino acid sequencing. It was demonstrated recently by A. S. Bhown, J. C. Bennett, P. H. Morgan, and J. E. Mole (1981, Anal. Biochem. 112, 158-162) that introduction of fluorescamine into the spinning cup reduced background by blocking primary amino groups at cycles where a proline residue is at the exposed amino terminus. A convenient blocking reaction program using o-phthalaldehyde which can be intercalated into the sequencing format of an automated Beckman liquid-phase sequencer is presented. The advantages of o-phthalaldehyde in blocking of primary amines when proline is amino terminal arise from its stability in aqueous solution and the ease of programmed metering of delivery to the sequencer spinning cup. The blocking reaction proved successful not only in extending sequence analyses but also in the elimination of unwanted sequences in selected peptide mixtures without the necessity of purification of the target peptide.
在埃德曼降解法的裂解步骤中产生的背景信号是进行长序列自动氨基酸测序的主要障碍。最近,A. S. 布翁、J. C. 贝内特、P. H. 摩根和J. E. 莫尔(1981年,《分析生物化学》第112卷,第158 - 162页)证明,在转杯中引入荧光胺,通过在脯氨酸残基位于暴露氨基末端的循环中封闭伯氨基,可降低背景信号。本文介绍了一种使用邻苯二甲醛的便捷封闭反应程序,该程序可插入到贝克曼自动液相测序仪的测序流程中。当脯氨酸位于氨基末端时,邻苯二甲醛在封闭伯胺方面的优势源于其在水溶液中的稳定性以及易于通过程序控制向测序仪转杯输送的计量方式。该封闭反应不仅成功地延长了序列分析,还能在无需纯化目标肽的情况下,消除选定肽混合物中不需要的序列。