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After cleavage sulfur deprotection for the convergence of protein synthesis by chemical linking

机译:裂解硫脱保护后,通过化学键合使蛋白质合成趋于一致

摘要

The present invention provides methods and compositions for the synthesis of polypeptides or oligopeptides by convergent assembly of the oligonucleotide pairs in a chemical ligation reaction. A significant aspect of the present invention, it is an oligopeptide with which can spontaneously generate the free C-terminal thioester moiety is deprotected, a C-terminal disulfide protected carboxy thioester group. This allows for the single precursor is involved in the chemical coupling reaction sequence, whereby it becomes possible to convergent synthetic approach. Are useful in methods for the chemical synthesis of oligopeptides, polypeptides and, by using peptide fragments of 4 or more particularly, the present invention is to assemble a product of oligopeptides or polypeptides, In the case, I will improve the efficiency of chemical ligation of the native.
机译:本发明提供了通过在化学连接反应中收敛组装寡核苷酸对来合成多肽或寡肽的方法和组合物。在本发明的一个重要方面,它是一种寡肽,它可以自发地生成被脱保护的游离的C端硫酯基团,一个C端的二硫键保护的羧基硫酯基团。这允许单一前体参与化学偶联反应序列,从而有可能会聚合成方法。可用于化学合成寡肽,多肽的方法,并且特别是通过使用4个或更多个肽段,本发明是组装寡肽或多肽的产物,在这种情况下,我将提高寡核苷酸或多肽的化学连接效率本地人。

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