Arginine-rich cell-penetrating peptides

被引:418
|
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
相关论文
共 50 条
  • [1] Arginine-rich cell-penetrating peptides with uncharged antisense oligomers
    Moulton, HM
    Moulton, JD
    DRUG DISCOVERY TODAY, 2004, 9 (20) : 870 - 870
  • [2] Guanidinylated chitosan inspired by arginine-rich cell-penetrating peptides
    Izawa, Hironori
    Kinai, Mizuki
    Ifuku, Shinsuke
    Morimoto, Minoru
    Saimoto, Hiroyuki
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2019, 125 : 901 - 905
  • [3] Interaction of Arginine-Rich Cell-Penetrating Peptides with an Artificial Neuronal Membrane
    Mucha, Piotr
    Sikorska, Emilia
    Rekowski, Piotr
    Ruczynski, Jaroslaw
    CELLS, 2022, 11 (10)
  • [4] The Uptake of Arginine-Rich Cell-Penetrating Peptides: Putting the Puzzle Together
    Brock, Roland
    BIOCONJUGATE CHEMISTRY, 2014, 25 (05) : 863 - 868
  • [5] Effect of helicity and hydrophobicity on cell-penetrating ability of arginine-rich peptides
    Oba, Makoto
    Nakajima, Shun
    Misao, Kurumi
    Yokoo, Hidetomo
    Tanaka, Masakazu
    BIOORGANIC & MEDICINAL CHEMISTRY, 2023, 91
  • [6] Gene transport and expression by arginine-rich cell-penetrating peptides in Paramecium
    Dai, Yun-Hao
    Liu, Betty Revon
    Chiang, Huey-Jenn
    Lee, Han-Jung
    GENE, 2011, 489 (02) : 89 - 97
  • [7] CHEMICAL AND BIOLOGICAL FACTORS THAT CONTRIBUTE TO THE INTERNALIZATION OF ARGININE-RICH CELL-PENETRATING PEPTIDES
    Futaki, Shiroh
    JOURNAL OF GENE MEDICINE, 2010, 12 (12): : 1015 - 1015
  • [8] Insights into Translocation of Arginine-Rich Cell-Penetrating Peptides across a Model Membrane
    Choe, Seungho
    JOURNAL OF PHYSICAL CHEMISTRY B, 2024, 128 (44): : 10894 - 10903
  • [9] Hemopexin as a Potential Binding Partner of Arginine-Rich Cell-Penetrating Peptides in Serum
    Nomura, Kayo
    Kawano, Kenichi
    Kawaguchi, Yoshimasa
    Kawamura, Yuki
    Michibata, Junya
    Kuwata, Keiko
    Sugiyama, Koji
    Kusumoto, Kenji
    Futaki, Shiroh
    ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE, 2022, : 603 - 615
  • [10] Protein transduction into the mouse otocyst using arginine-rich cell-penetrating peptides
    Miwa, Toru
    Minoda, Ryosei
    Kaitsuka, Taku
    Ise, Momoko
    Tomizawa, Kazuhito
    Yumoto, Eiji
    NEUROREPORT, 2011, 22 (18) : 994 - 999