大规模多针肽合成。

Peptide research Pub Date : 1995-01-01
N J Maeji, A M Bray, R M Valerio, W Wang
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引用次数: 0

摘要

多针肽合成方法起源于抗原表位定位的免疫学工具。然而,基础技术的不断发展使得合成的规模达到每引脚10 μ mol。在这种情况下,该方法不能再仅仅被认为是一种筛选工具。通过合成2913种不同的多肽,评估了该方法的总体合成效率,这些多肽的序列同源性很少或没有同源性,长度最长可达46-mer。对粗肽进行高效液相色谱分析,表明合成产物的整体质量较高。该方法适用于多毫克合成多肽,而不牺牲96孔格式的任何固有优点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Larger scale multipin peptide synthesis.

The multipin peptide synthesis approach originated as an immunological tool for epitope mapping. However, continuing evolution of the basic technology has allowed synthesis at scales up to 10 mumol per pin. At this loading, the methodology can no longer be considered just a screening tool. The overall synthesis efficiency of this approach was assessed by the synthesis of 2913 different peptides having little or no sequence homology and ranging up to a 46-mer in length. High performance liquid chromatography analysis of the crude peptides indicates overall quality of synthesis was high. The method is suitable for multi-milligram synthesis of peptides without sacrificing any of the inherent advantages of the 96-well format.

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