Borgia J A, Malkar N B, Abbasi H U, Fields G B
Department of Chemistry & Biochemistry, Florida Atlantic University, Boca Raton, FL 33431-0991, USA.
J Biomol Tech. 2001 Sep;12(3):44-68.
Methods for the efficient solid-phase synthesis of glycopeptides have developed rapidly over the past two decades. Incorporation of both O- and N-linked glycosides, as well as branched carbohydrates, into peptides is readily achieved. Synthetic glycoproteins of modest size have also been constructed. As glycopeptide synthesis protocols have progressed, so has the recognition of distinct categories of synthetic difficulties. Such categories include (a) unstable glycosidic linkages, (b) multifunctional amino acids not easily glycosylated and incorporated into peptides, and (c) glycosylated peptide sequences that are subject to side reactions. In the present overview,we describe specific examples for each category of problematic glycopeptide syntheses, as well as solutions to these problems.
在过去二十年中,高效的糖肽固相合成方法发展迅速。将O-连接和N-连接的糖苷以及支链碳水化合物掺入肽中很容易实现。中等大小的合成糖蛋白也已构建出来。随着糖肽合成方案的进展,对不同类别的合成困难的认识也在增加。这些类别包括:(a)不稳定的糖苷键;(b)不易糖基化并掺入肽中的多功能氨基酸;(c)易发生副反应的糖基化肽序列。在本综述中,我们描述了每类有问题的糖肽合成的具体例子以及这些问题的解决方案。