Antisense effects of DNA-peptide conjugates.

Takanori Kubo, Rumiana Bakalova, Hideki Ohba, Masayuki Fujii
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引用次数: 8

Abstract

Antisense conjugate DNA covalently bound to functional amines, sugars or peptides such as nuclear localization signals (NLS), nuclear export signals (NES) and artificial amphiphilic alpha-helical and beta-sheet peptides were synthesized by solid phase fragment condensation (SPFC). Inhibitory effects on human telomerase of synthesized antisense conjugate DNAs were evaluated by TRAP assay. Antisense conjugate DNAs showed several times higher inhibitory effects on telomerase activity compared to native antisense DNA in cell lysis solutions. Antisense conjugate DNAs showed comparable or higher as same as inhibitory activity compared with antisense phosphorothioate DNA (S-DNA). Interestingly, antisense conjugate DNA showed much higher inhibition against telomerase activity with native antisense DNA or antisense phosphorothioate DNA in cellular system. We observed enhanced cellular uptake and positively controlled intracellular localization of conjugate DNAs by use of confocal fluorescent microscope.

dna -肽偶联物的反义作用。
采用固相片段缩合(SPFC)技术合成了与功能胺、糖或肽共价结合的反义共轭DNA,如核定位信号(NLS)、核输出信号(NES)和人工两亲性α -螺旋肽和β -片肽。用TRAP法评价合成的反义结合dna对人端粒酶的抑制作用。在细胞裂解液中,反义结合DNA对端粒酶活性的抑制作用比天然反义DNA高几倍。与反义硫代DNA (S-DNA)相比,反义共轭DNA表现出相当或更高的抑制活性。有趣的是,在细胞系统中,反义结合DNA与天然反义DNA或反义硫代DNA对端粒酶活性的抑制作用要高得多。通过共聚焦荧光显微镜观察到细胞对共轭dna的摄取增强,细胞内定位正向控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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