Cell-penetrating peptides:: mechanism and kinetics of cargo delivery

被引:655
作者
Zorko, M
Langel, Ü
机构
[1] Univ Ljubljana, Fac Med, Inst Biochem, SLO-1000 Ljubljana, Slovenia
[2] Stockholm Univ, Arrhenius Lab, Dept Neurochem & Neurotoxicol, SE-10691 Stockholm, Sweden
关键词
drug delivery; membrane translocation; cellular uptake; endocytosis; toxicity;
D O I
10.1016/j.addr.2004.10.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cell-penetrating peptides (CPPs) are short peptides of less than 30 amino acids that are able to penetrate cell membranes and translocate different cargoes into cells. The only common feature of these peptides appears to be that they are amphipathic and net positively charged. The mechanism of cell translocation is not known but it is apparently receptor and energy independent although, in certain cases, translocation can be partially mediated by endocytosis. Cargoes that are successfully internalized by CPPs range from small molecules to proteins and supramolecular particles. Most CPPs are inert or have very limited side effects. Their penetration into cells is rapid and initially first-order, with half-times from 5 to 20 min. The size of smaller cargoes does not affect the rate of internalization, but with larger cargoes, the rate is substantially decreased. CPPs are novel vehicles for the translocation of cargo into cells, whose properties make them potential drug delivery agents, of interest for future use. (c) 2004 Elsevier B.V All rights reserved.
引用
收藏
页码:529 / 545
页数:17
相关论文
共 96 条
[41]   Cell-penetrating peptides [J].
Lindgren, M ;
Hallbrink, M ;
Prochiantz, A ;
Langel, U .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (03) :99-103
[42]   Passage of cell-penetrating peptides across a human epithelial cell layer in vitro [J].
Lindgren, ME ;
Hällbrink, MM ;
Elmquist, AM ;
Langel, Ü .
BIOCHEMICAL JOURNAL, 2004, 377 :69-76
[43]   Mechanism of peptide-induced mast cell degranulation - Translocation and patch-clamp studies [J].
Lorenz, D ;
Wiesner, B ;
Zipper, J ;
Winkler, A ;
Krause, E ;
Beyermann, M ;
Lindau, M ;
Bienert, M .
JOURNAL OF GENERAL PHYSIOLOGY, 1998, 112 (05) :577-591
[44]  
LUM BL, 1993, PHARMACOTHERAPY, V13, P88
[45]  
Mahato RI, 1999, CURR OPIN MOL THER, V1, P226
[46]   Polyarginine enters cells more efficiently than other polycationic homopolymers [J].
Mitchell, DJ ;
Kim, DT ;
Steinman, L ;
Fathman, CG ;
Rothbard, JB .
JOURNAL OF PEPTIDE RESEARCH, 2000, 56 (05) :318-325
[47]   A novel potent strategy for gene delivery using a single peptide vector as a carrier [J].
Morris, MC ;
Chaloin, L ;
Méry, J ;
Heitz, F ;
Divita, G .
NUCLEIC ACIDS RESEARCH, 1999, 27 (17) :3510-3517
[48]   A new peptide vector for efficient delivery of oligonucleotides into mammalian cells [J].
Morris, MC ;
Vidal, P ;
Chaloin, L ;
Heitz, F ;
Divita, G .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2730-2736
[50]  
NEKHOTIAEVA N, 2003, FABEB J, V17, pU549