Cell-penetrating peptides as delivery vehicles for biology and medicine

被引:335
作者
Stewart, Kelly M. [2 ]
Horton, Kristin L. [2 ]
Kelley, Shana O. [1 ,2 ]
机构
[1] Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON, Canada
[2] Univ Toronto, Fac Med, Dept Biochem, Toronto, ON, Canada
关键词
D O I
10.1039/b719950c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cell-penetrating peptides (CPPs) have found numerous applications in biology and medicine since the first synthetic cell-permeable sequence was identified two decades ago. Numerous types of drugs have been transported into cells using CPPs, including small-molecule pharmaceuticals, therapeutic proteins, and antisense oligonucleotides. Improved agents for medical imaging have been generated by conjugation with CPPs, with the appended peptides promoting cellular uptake and in some cases, cell-type specificity. Organelle-specific CPPs have also been generated, providing a means to target specific subcellular sites. This review highlights achievements in this area and illustrates the numerous examples where peptide chemistry was exploited as a means to provide new tools for biology and medicine.
引用
收藏
页码:2242 / 2255
页数:14
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共 200 条
[1]   Treatment of ischemic brain damage by perturbing NMDA receptor-PSD-95 protein interactions [J].
Aarts, M ;
Liu, YT ;
Liu, LD ;
Besshoh, S ;
Arundine, M ;
Gurd, JW ;
Wang, YT ;
Salter, MW ;
Tymianski, M .
SCIENCE, 2002, 298 (5594) :846-850
[2]   Efficient splicing correction by PNA conjugation to an R6-Penetratin delivery peptide [J].
Abes, Said ;
Turner, John J. ;
Ivanova, Gabriela D. ;
Owen, David ;
Williams, Donna ;
Arzumanov, Andrey ;
Clair, Philippe ;
Gait, Michael J. ;
Lebleu, Bernard .
NUCLEIC ACIDS RESEARCH, 2007, 35 (13) :4495-4502
[3]   Vectorization of morpholino oligomers by the (R-Ahx-R)4 peptide allows efficient splicing correction in the absence of endosomolytic agents [J].
Abes, Said ;
Moulton, Hong M. ;
Clair, Philippe ;
Prevot, Paul ;
Youngblood, Derek S. ;
Wu, Rebecca P. ;
Iversen, Patrick L. ;
Lebleu, Bernard .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (03) :304-313
[4]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[5]   Inhibition of NF-κB activation by peptides targeting NF-κB essential modulator (NEMO) oligomerization [J].
Agou, F ;
Courtois, G ;
Chiaravalli, J ;
Baleux, F ;
Coïc, YM ;
Traincard, F ;
Israël, A ;
Véron, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (52) :54248-54257
[6]   Enhancement of phage-mediated gene transfer by nuclear localization signal [J].
Akuta, T ;
Eguchi, A ;
Okuyama, H ;
Senda, T ;
Inokuchi, H ;
Suzuki, Y ;
Nagoshi, E ;
Mizuguchi, H ;
Hayakawa, T ;
Takeda, K ;
Hasegawa, M ;
Nakanishi, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 297 (04) :779-786
[7]   Semiconductor clusters, nanocrystals, and quantum dots [J].
Alivisatos, AP .
SCIENCE, 1996, 271 (5251) :933-937
[8]   Cellular delivery of MRI contrast agents [J].
Allen, MJ ;
MacRenaris, KW ;
Venkatasubramanian, PN ;
Meade, TJ .
CHEMISTRY & BIOLOGY, 2004, 11 (03) :301-307
[9]   Synthesis and visualization of a membrane-permeable MRI contrast agent [J].
Allen, MJ ;
Meade, TJ .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2003, 8 (07) :746-750
[10]   In vivo fluorescence imaging for tissue diagnostics [J].
AnderssonEngels, S ;
afKlinteberg, C ;
Svanberg, K ;
Svanberg, S .
PHYSICS IN MEDICINE AND BIOLOGY, 1997, 42 (05) :815-824