TAT-RasGAP<sub>317-326</sub> kills cells by targeting inner-leaflet-enriched phospholipids.
Détails
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Accès restreint UNIL
Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
Accès restreint UNIL
Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
ID Serval
serval:BIB_304AC399FABC
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
TAT-RasGAP<sub>317-326</sub> kills cells by targeting inner-leaflet-enriched phospholipids.
Périodique
Proceedings of the National Academy of Sciences of the United States of America
ISSN
1091-6490 (Electronic)
ISSN-L
0027-8424
Statut éditorial
Publié
Date de publication
15/12/2020
Peer-reviewed
Oui
Volume
117
Numéro
50
Pages
31871-31881
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
TAT-RasGAP <sub>317-326</sub> is a cell-penetrating peptide-based construct with anticancer and antimicrobial activities. This peptide kills a subset of cancer cells in a manner that does not involve known programmed cell death pathways. Here we have elucidated the mode of action allowing TAT-RasGAP <sub>317-326</sub> to kill cells. This peptide binds and disrupts artificial membranes containing lipids typically enriched in the inner leaflet of the plasma membrane, such as phosphatidylinositol-bisphosphate (PIP <sub>2</sub> ) and phosphatidylserine (PS). Decreasing the amounts of PIP <sub>2</sub> in cells renders them more resistant to TAT-RasGAP <sub>317-326</sub> , while reducing the ability of cells to repair their plasma membrane makes them more sensitive to the peptide. The W317A TAT-RasGAP <sub>317-326</sub> point mutant, known to have impaired killing activities, has reduced abilities to bind and permeabilize PIP <sub>2</sub> - and PS-containing membranes and to translocate through biomembranes, presumably because of a higher propensity to adopt an α-helical state. This work shows that TAT-RasGAP <sub>317-326</sub> kills cells via a form of necrosis that relies on the physical disruption of the plasma membrane once the peptide targets specific phospholipids found on the cytosolic side of the plasma membrane.
Mots-clé
Animals, CHO Cells, Cell Death/drug effects, Cell Membrane/drug effects, Cell Membrane/metabolism, Cell Membrane/ultrastructure, Cricetulus, GTPase-Activating Proteins/pharmacology, GTPase-Activating Proteins/therapeutic use, HeLa Cells, Humans, Liposomes/metabolism, Liposomes/ultrastructure, Microscopy, Electron, Molecular Dynamics Simulation, Neoplasms/drug therapy, Nuclear Magnetic Resonance, Biomolecular, Peptide Fragments/pharmacology, Peptide Fragments/therapeutic use, Phosphatidylinositol 4,5-Diphosphate/metabolism, Phosphatidylserines/metabolism, anticancer peptides, cell-penetrating peptides, membranolytic peptides, phosphatidylserine, phosphoinositides
Pubmed
Web of science
Création de la notice
07/12/2020 14:32
Dernière modification de la notice
16/07/2021 5:37