Medium-sized peptides as built in carriers for biologically active compounds

被引:43
作者
Hudecz, F
Bánóczi, Z
Csík, G
机构
[1] Eotvos Lorand Univ, Hungarian Acad Sci, Res Grp Peptide Chem, H-1518 Budapest, Hungary
[2] Eotvos Lorand Univ, Dept Organ Chem, H-1518 Budapest, Hungary
[3] Semmelweis Univ, Inst Biophys & Radiat Biol, H-1444 Budapest, Hungary
关键词
cell penetrating peptides; intracellular delivery of peptides; oligonucleotides; PNA; reporter molecules and drugs; fusion proteins with translocation sequence;
D O I
10.1002/med.20034
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A growing number of oligopeptides of natural and/or synthetic origin have been described and considered as targeting structures for delivery bioactive compounds into various cell types. This review will outline the discovery of peptide sequences and the corresponding mid-sized oligopeptides with membrane translocating properties and also summarize de novo designed structures possessing similar features. Conjugates and chimera constructs derived from these sequences with covalently attached bioactive peptide, epitope, oligonucleotide, PNA, drug, reporter molecule will be reviewed. A brief note will refer to the present understanding on the uptake mechanism at the end of each section. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:679 / 736
页数:58
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