Cell-penetrating peptides, electroporation and drug delivery

被引:18
作者
Cahill, K. [1 ]
机构
[1] Univ New Mexico, Dept Phys & Astron, Biophys Grp, Albuquerque, NM 87131 USA
关键词
HUMAN IMMUNODEFICIENCY VIRUS; TAT-FUSION PROTEINS; ELECTRICAL BREAKDOWN; MAMMALIAN-CELLS; PLASMA-MEMBRANE; LIPID-MEMBRANES; TUMOR-GROWTH; TRANSLOCATION; TRANSDUCTION; ANTAGONISTS;
D O I
10.1049/iet-syb.2010.0007
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Certain short polycations, such as trans-activating transcriptional activator and oligoarginine, rapidly pass through the plasma membranes of mammalian cells by a mechanism called transduction, as well as by endocytosis and macropinocytosis. These cell-penetrating peptides can carry with them cargos of 30 amino acids, more than the nominal limit of 500 Da and enough to be therapeutic. An analysis of the electrostatics of a charge outside the cell membrane and some recent experiments suggest that transduction may proceed by molecular electroporation. Ways to target diseased cells, rather than all cells, are discussed.
引用
收藏
页码:367 / 378
页数:12
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