Yuankun Dao , Weidong Dong , Jun Zhang , Suwei Dong
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引用次数: 0
Abstract
N-glycans in eukaryotic proteins are commonly attached to asparagine residues via β-N-glycosidic linkages, which are susceptible to glycosidases, such as PNGase. Here we report the preparation of α-N-glycosylated peptides based on the solid-phase peptide synthesis strategy using an α-N-GlcNAc-containing asparagine building block, and a transglycosylation reaction of oligosaccharide oxazoline promoted by endoglycosidases CCN180H. The resultant glycopeptide, bearing the complex-type α-N-sialyl undecasaccharide, exhibits resistance against PNGase F, which may be of potential use in studying the catabolism of N-glycans and glycoengineering those peptide-based therapeutics.
真核蛋白中的n -聚糖通常通过β- n -糖苷键连接到天冬酰胺残基上,这对糖苷酶(如PNGase)很敏感。本研究以含α- n - glcnac的天冬酰胺为基础,采用固相多肽合成策略制备了α- n -糖基化多肽,并在内糖苷酶CCN180H的催化下进行了低聚糖恶唑啉的转糖基化反应。合成的糖肽含有α- n -唾液醇脱糖复合物,对PNGase F具有抗性,这可能在研究n -聚糖的分解代谢和糖工程治疗中具有潜在的应用价值。
期刊介绍:
The Journal of Carbohydrate Chemistry serves as an international forum for research advances involving the chemistry and biology of carbohydrates. The following aspects are considered to fall within the scope of this journal:
-novel synthetic methods involving carbohydrates, oligosaccharides, and glycoconjugates-
the use of chemical methods to address aspects of glycobiology-
spectroscopic and crystallographic structure studies of carbohydrates-
computational and molecular modeling studies-
physicochemical studies involving carbohydrates and the chemistry and biochemistry of carbohydrate polymers.