Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells

被引:64
作者
Wang, Ya-Hui
Chen, Chung-Pin
Chan, Ming-Huan
Chang, Microsugar
Hou, Yu-Wun
Chen, Hwei-Hsien
Hsu, Hui-Ru
Liu, Kevin
Lee, Han-Jung [1 ]
机构
[1] Natl Dong Hwa Univ, Dept Life Sci, Hualien 97401, Taiwan
[2] Tzu Chi Univ, Inst Pharmacol & Toxicol, Hualien 97004, Taiwan
关键词
protein transduction domain; cell penetrating peptide; cellular internalization; green fluorescent protein; transdermal delivery; STEROID-RECEPTOR SUPERFAMILY; HUMAN IMMUNODEFICIENCY VIRUS; TR2 ORPHAN RECEPTOR; MAJOR LATE PROMOTER; TRANSLOCATION MECHANISMS; PENETRATING PEPTIDES; GENE-EXPRESSION; CELLULAR UPTAKE; TAT PEPTIDE; TRANSDUCTION;
D O I
10.1016/j.bbrc.2006.05.205
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
Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or P-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:758 / 767
页数:10
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