Arginine-rich cell-penetrating peptides

被引:423
作者
Schmidt, Nathan [1 ]
Mishra, Abhijit [2 ]
Lai, Ghee Hwee [1 ]
Wong, Gerard C. L. [1 ,2 ]
机构
[1] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
TAT; Polyarginine; Cell-penetrating peptides; Protein transduction domain; Membranes; Drug delivery; TAT-FUSION PROTEINS; SUBSEQUENT INTRACELLULAR TRAFFICKING; HUMAN IMMUNODEFICIENCY VIRUS; HEPARAN-SULFATE; DEPENDENT TRANSLOCATION; MOLECULAR TRANSPORTERS; TRYPTOPHAN FLUORESCENCE; COUNTERION CONDENSATION; TRANSDUCTION DOMAINS; MEMBRANE CURVATURE;
D O I
10.1016/j.febslet.2009.11.046
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
Arginine-rich cell-penetrating peptides are short cationic peptides capable of traversing the plasma membranes of eukaryotic cells. While successful intracellular delivery of many biologically active macromolecules has been accomplished using these peptides, their mechanisms of cell entry are still under investigation. Recent dialogue has centered on a debate over the roles that direct translocation and endocytotic pathways play in internalization of cell-penetrating peptides. In this paper, we review the evidence for the broad range of proposed mechanisms, and show that each distinct process requires negative Gaussian membrane curvature as a necessary condition. Generation of negative Gaussian curvature by cell-penetrating peptides is directly related to their arginine content. We illustrate these concepts using HIV TAT as an example. (C) 2009 Published by Elsevier B. V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:1806 / 1813
页数:8
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