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Arginine-rich cell-penetrating peptides induce membrane multilamellarity and subsequently enter via formation of a fusion pore

  1. 1.
    0498461 - ÚOCHB 2019 RIV US eng J - Článek v odborném periodiku
    Allolio, Christoph - Magarkar, Aniket - Jurkiewicz, Piotr - Baxová, Katarína - Javanainen, Matti - Mason, Philip E. - Šachl, Radek - Cebecauer, Marek - Hof, Martin - Horinek, D. - Heinz, V. - Rachel, R. - Ziegler, C. M. - Schröfel, A. - Jungwirth, Pavel
    Arginine-rich cell-penetrating peptides induce membrane multilamellarity and subsequently enter via formation of a fusion pore.
    Proceedings of the National Academy of Sciences of the United States of America. Roč. 115, č. 47 (2018), s. 11923-11928. ISSN 0027-8424. E-ISSN 1091-6490
    Grant CEP: GA ČR(CZ) GA16-01074S; GA ČR GA17-03160S
    Institucionální podpora: RVO:61388963 ; RVO:61388955
    Klíčová slova: cell-penetrating peptide * membrane fusion * fluorescence microscopy * electron microscopy * molecular dynamics
    Obor OECD: Physical chemistry; Physical chemistry (UFCH-W)
    Impakt faktor: 9.580, rok: 2018
    https://www.pnas.org/content/115/47/11923

    Arginine-rich cell-penetrating peptides do not enter cells by directly passing through a lipid membrane, they instead passively enter vesicles and live cells by inducing membrane multilamellarity and fusion. The molecular picture of this penetration mode, which differs qualitatively from the previously proposed direct mechanism, is provided by molecular dynamics simulations. The kinetics of vesicle agglomeration and fusion by an iconic cell-penetrating peptide-nonaarginine-are documented via real-time fluorescence techniques, while the induction of multilamellar phases in vesicles and live cells is demonstrated by a combination of electron and fluorescence microscopies. This concert of experiments and simulations reveals that the identified passive cell penetration mechanism bears analogy to vesicle fusion induced by calcium ions, indicating that the two processes may share a common mechanistic origin.
    Trvalý link: http://hdl.handle.net/11104/0290827

     
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