Biological applications of protein transduction technology

被引:79
作者
Kabouridis, PS [1 ]
机构
[1] Univ London, Queen Marys Sch Med & Dent, William Harvey Res Inst, Bone & Joint Res Unit, London EC1M 6BQ, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tibtech.2003.09.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The impermeable nature of the cell membrane to peptides, proteins, DNA and oligonucleotides limits the therapeutic potential of these biological agents. However, the recent discovery of short cationic peptides that cross the plasma membrane efficiently is opening up new possibilities for the intracellular delivery of such agents. These peptides are commonly referred to as protein transduction domains (PTDs) and are successfully used to transport heterologous proteins, peptides and other types of cargo into cells. Several recent reports have used the membrane transducing technology in vivo to deliver biologically active cargo into various tissues. This review discusses the structure of the most commonly used PTDs and how their ability to transduce membranes is used to regulate biological functions. It also considers future directions and the potential of this technology to move from the laboratory into the clinic.
引用
收藏
页码:498 / 503
页数:6
相关论文
共 78 条
[1]   TAT fusion proteins containing tyrosine 42-deleted IκBα arrest osteoclastogenesis [J].
Abu-Amer, Y ;
Dowdy, SF ;
Ross, FP ;
Clohisy, JC ;
Teitelbaum, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (32) :30499-30503
[2]   TAT-mediated protein transduction into mammalian cells [J].
Becker-Hapak, M ;
McAllister, SS ;
Dowdy, SF .
METHODS, 2001, 24 (03) :247-256
[3]   In vivo delivery of the caveolin-1 scaffolding domain inhibits nitric oxide synthesis and reduces inflammation [J].
Bucci, M ;
Gratton, JP ;
Rudic, RD ;
Acevedo, L ;
Roviezzo, F ;
Cirino, G ;
Sessa, WC .
NATURE MEDICINE, 2000, 6 (12) :1362-1367
[4]   Transloading of tumor antigen-derived peptides into antigen-presenting cells [J].
Buschle, M ;
Schmidt, W ;
Zauner, W ;
Mechtler, K ;
Trska, B ;
Kirlappos, H ;
Birnstiel, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :3256-3261
[5]  
Cao GD, 2002, J NEUROSCI, V22, P5423
[6]   Intracellular delivery of a Tat-eGFP fusion protein into muscle cells [J].
Caron, NJ ;
Torrente, Y ;
Camirand, G ;
Bujold, M ;
Chapdelaine, P ;
Leriche, K ;
Bresolin, N ;
Tremblay, JP .
MOLECULAR THERAPY, 2001, 3 (03) :310-318
[7]   Evidence of protein transduction but Not intercellular transport by proteins fused to HIV tat in retinal cell culture and in vivo [J].
Cashman, SM ;
Morris, DJ ;
Kumar-Singh, R .
MOLECULAR THERAPY, 2003, 8 (01) :130-142
[8]  
Celis JE, 1986, MICROINJECTION ORGAN
[9]  
Chang D.C., 1991, GUIDE ELECTROPORATIO
[10]  
COHENSAIDON C, IN PRESS BLOOD