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肽模拟物:一种用于制备多种组合肽模拟物珠文库的通用方法。

Peptomers: a versatile approach for the preparation of diverse combinatorial peptidomimetic bead libraries.

作者信息

Ostergaard S, Holm A

机构信息

Novo Research Institute, Bagsvaerd, Denmark.

出版信息

Mol Divers. 1997;3(1):17-27. doi: 10.1023/a:1009698507588.

Abstract

This report describes a versatile approach in the generation of peptidomimetic bead libraries. The method is based on the preparation of peptide-peptoid hybrids using the portioning-mixing procedure, which gives diverse peptidomimetic bead libraries composed of peptides, peptoids and peptide-peptoid hybrids. We term these peptomers, from peptide-peptoid hybrid polymers. The synthesis of the peptomers is easily accomplished by adapting the peptoid synthesis strategy, in which a primary amine reacts with bromoacetic acid, and we combine this methodology with conventional peptide synthesis. The sequence of the active compound is deduced by conventional microsequencing using Edman degradation chemistry, thus avoiding the synthesis of a coding structure or the addition of molecular tags. We demonstrate the utility of the peptomer approach by the synthesis of a bead library together with the identification of novel peptidomimetic ligands binding to the macromolecular targets streptavidin and the insulin receptor.

摘要

本报告描述了一种在生成拟肽珠文库方面通用的方法。该方法基于使用分配-混合程序制备肽-类肽杂合物,从而得到由肽、类肽和肽-类肽杂合物组成的多样拟肽珠文库。我们将这些来自肽-类肽杂合聚合物的物质称为肽聚体。肽聚体的合成通过调整类肽合成策略很容易实现,其中伯胺与溴乙酸反应,并且我们将这种方法与传统肽合成相结合。活性化合物的序列通过使用埃德曼降解化学的传统微量测序推导得出,从而避免了编码结构的合成或分子标签的添加。我们通过合成一个珠文库以及鉴定与大分子靶标链霉亲和素和胰岛素受体结合的新型拟肽配体,证明了肽聚体方法的实用性。

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