[GnRH类似物的合成及其在靶向基因传递系统中的应用]。

Bioorganicheskaia khimiia Pub Date : 2012-01-01
T V Iablokova, P S Chelushkin, M Iu Dorosh, A M Efremov, S V Orlov, S V Burov
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引用次数: 0

摘要

采用固相肽合成和化学结扎技术合成了一组含有SV-40病毒大t抗原核定位信号(NLS)的GnRH类似物。NLS酰肼与丙酮酸修饰的GnRH类似物在相互作用过程中形成腙,实现了选择性化学连接。通过转染报告型荧光素酶和β -半乳糖苷酶基因或自杀型HSV-1胸苷激酶基因的人癌细胞实验,证明了合成多肽载体的效率。研究表明,通过GnRH受体介导的内吞作用途径,肽/DNA复合物穿透细胞膜,可以实现对癌细胞的选择性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Synthesis of GnRH analogs and their application in targeted gene delivery systems].

A set of GnRH analogues containing nuclear localization signal (NLS) of SV-40 virus large T-antigen have been synthesized using solid phase peptide synthesis and chemical ligation technique. Selective chemical ligation was achieved as a result of hydrazone formation in the course of interaction between NLS hydrazide and GnRH analog modified by pyruvic acid. The efficiency of synthesized peptide carriers was demonstrated in experiments with human cancer cells transfected by reporter luciferase and beta-galactosidase genes or suicide HSV-1 thymidine kinase gene. It was shown that selectivity of action on cancer cells can be achieved as a result of peptide/DNA complex penetration through the cell membrane by GnRH receptor-mediated endocytosis pathway.

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