The Delivery of Biologically Active (Therapeutic) Peptides and Proteins into Cells

被引:39
作者
Grdisa, M. [1 ]
机构
[1] Rudjer Boskovic Inst, Div Mol Med, Zagreb 10000, Croatia
关键词
Drug delivery; protein transduction; TAT; amphipathic peptides; CPP; CTP; ARGININE-RICH PEPTIDES; EMBRYONIC STEM-CELLS; CYTOPLASMIC TRANSDUCTION PEPTIDE; HUMAN IMMUNODEFICIENCY VIRUS; TAT-MEDIATED TRANSDUCTION; ISCHEMIC BRAIN INJURY; CELLULAR UPTAKE; PENETRATING PEPTIDES; IN-VIVO; INTRACELLULAR DELIVERY;
D O I
10.2174/092986711795029591
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
Biologically active peptides and proteins have a great potential to act as targeted drug therapies in the treatment of a variety of diseases, including cancer. However, their use in vivo is limited by their low stability and cell permeability. Thus, it is necessary to develop efficient and safe peptide/protein delivery systems that can overcome these problems and increase a therapy's bioavailability. The search for promising vectors has led to the use of compounds called cell-penetrating peptides or protein transduction domains. The cell-penetrating peptides, as effective transporter, are utilized to enhance uptake of various biologically active peptide/protein cargos upon fusion or attachment to its sequences. Cell-penetrating peptides have been the subject of investigation of many researchers, however this review only focuses on the arginine-rich and amphipathic carriers and their potential therapeutic use.
引用
收藏
页码:1373 / 1379
页数:7
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