Haralambidis J, Duncan L, Angus K, Tregear G W
Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.
Nucleic Acids Res. 1990 Feb 11;18(3):493-9. doi: 10.1093/nar/18.3.493.
We have developed methods for the synthesis of peptide-oligodeoxyribonucleotide conjugate molecules in particular, and polyamide-oligonucleotide conjugates in general. Synthesis is carried out by a solid-phase procedure and involves the assembly of a polyamide on the solid support, conversion of the terminal amino group to a protected primary aliphatic hydroxy group by reaction with alpha, omega-hydroxycarboxylic acid derivatives, and finally oligonucleotide synthesis using phosphoramidite chemistry. The conjugate molecules can be used as DNA probes, with the polyamide component carrying one or more non-radioactive markers. These conjugates also have the potential to be used as anti-sense inhibitors of gene expression, with the peptide segment acting as a targeting moiety.
我们已经开发出了合成肽 - 寡脱氧核糖核苷酸共轭分子的方法,特别是合成聚酰胺 - 寡核苷酸共轭物的通用方法。合成通过固相程序进行,包括在固相载体上组装聚酰胺,通过与α,ω - 羟基羧酸衍生物反应将末端氨基转化为受保护的伯脂肪族羟基,最后使用亚磷酰胺化学进行寡核苷酸合成。这些共轭分子可用作DNA探针,聚酰胺组分携带一个或多个非放射性标记。这些共轭物也有潜力用作基因表达的反义抑制剂,肽段作为靶向部分。