THE SYNTHESIS OF POLYAMIDE OLIGONUCLEOTIDE CONJUGATE MOLECULES

被引:79
作者
HARALAMBIDIS, J
DUNCAN, L
ANGUS, K
TREGEAR, GW
机构
[1] Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/18.3.493
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 α,ω-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. © 1990 Oxford University Press.
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页码:493 / 499
页数:7
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