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Cell-penetrating peptides: 20 years later, where do we stand?
被引:670
|作者:
Bechara, Cherine
[1
]
Sagan, Sandrine
[1
]
机构:
[1] Univ Paris 06, Lab BioMol, Cc 182, ENS,UMR CNRS 7203, F-75252 Paris 05, France
关键词:
Endocytosis;
Membrane translocation;
Glycosaminoglycans clustering;
Arginine;
Tryptophan;
ARGININE-RICH PEPTIDES;
TAT-FUSION PROTEINS;
PLASMA-MEMBRANE;
LIPID-BILAYERS;
ANTENNAPEDIA HOMEODOMAIN;
ANTIMICROBIAL PEPTIDES;
INTRACELLULAR DELIVERY;
3RD HELIX;
ANTISENSE OLIGONUCLEOTIDES;
INTERNALIZATION MECHANISMS;
D O I:
10.1016/j.febslet.2013.04.031
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:
Twenty years ago, the discovery of peptides able to cross cellular membranes launched a novel field in molecular delivery based on these non-invasive vectors, most commonly called cell-penetrating peptides (CPPs) or protein transduction domains (PTDs). These peptides were shown to efficiently transport various biologically active molecules inside living cells, and thus are considered promising devices for medical and biotechnological developments. Moreover, CPPs emerged as potential tools to study the prime mechanisms of cellular entry across the plasma membrane. This review is dedicated to CPP fundamentals, with an emphasis on the molecular requirements and mechanism of their entry into eukaryotic cells. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:1693 / 1702
页数:10
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