Covalent coupling of a PIM-1 oncogene targeted PNA with an antennapedia derived peptide

被引:5
作者
Bertrand, JR
Sumbatyan, N
Maivy, C
机构
[1] Inst Gustave Roussy, CNRS UMR 8121, F-94805 Villejuif, France
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow, Leninskie Gory, Russia
关键词
PNA; antenapedia peptide; penetratin; cell penetrating peptide; covalent conjugate; oncogene inhibition; pim-1;
D O I
10.1081/NCN-120023046
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
Peptide nucleic acids (PNA) are promising antisense molecule for blocking gene expression in cell culture or in vivo. Nevertheless because they are poor efficient to pass the cellular membrane, it is necessary to use a vectorisation agent to observe an inhibitory effect. We describe the coupling of the rhodamine labeled 17-mer antisense PNA to a fusogenic peptide from antenapedia via S-S linkage, the studies of the penetration of this complex into fibroblast cells and its inhibitory effect on piml targeted protononcogene.
引用
收藏
页码:1611 / 1613
页数:3
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