The role of spontaneous lipid curvature in the interaction of interfacially active peptides with membranes

被引:100
作者
Koller, Daniel [1 ]
Lohner, Karl [1 ]
机构
[1] Graz Univ, Inst Mol Biosci, Div Biophys, A-8042 Graz, Austria
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2014年 / 1838卷 / 09期
关键词
Antimicrobial peptide; Membrane interface; Membrane curvature; Membrane disruption; Inverse hexagonal phase; Non-lamellar (cubic) phase; CELL-PENETRATING PEPTIDES; LATERAL PRESSURE PROFILE; X-RAY-DIFFRACTION; ANTIMICROBIAL PEPTIDES; ESCHERICHIA-COLI; PORE FORMATION; BETA-SHEET; PHOSPHOCHOLINE CYTIDYLYLTRANSFERASE; ANTIBACTERIAL PEPTIDES; INTRINSIC CURVATURE;
D O I
10.1016/j.bbamem.2014.05.013
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
Research on antimicrobial peptides is in part driven by urgent medical needs such as the steady increase in pathogens being resistant to antibiotics. Despite the wealth of information compelling structure-function relationships are still scarce and thus the interfacial activity model has been proposed to bridge this gap. This model also applies to other interfacially active (membrane active) peptides such as cytolytic, cell penetrating or antitumor peptides. One parameter that is strongly linked to interfacial activity is the spontaneous lipid curvature, which is experimentally directly accessible. We discuss different parameters such as H-bonding, electrostatic repulsion, changes in monolayer surface area and lateral pressure that affect induction of membrane curvature, but also vice versa how membrane curvature triggers peptide response. In addition, the impact of membrane lipid composition on the formation of curved membrane structures and its relevance for diverse mode of action of interfacially active peptides and in turn biological activity are described. This article is part of a Special Issue entitled: Interfacially Active Peptides and Proteins. Guest Editors: William C. Wimley and Kalina Hristova. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:2250 / 2259
页数:10
相关论文
共 140 条
  • [1] Hydrogen-bond energetics drive helix formation in membrane interfaces
    Almeida, Paulo F.
    Ladokhin, Alexey S.
    White, Stephen H.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2012, 1818 (02): : 178 - 182
  • [2] Membrane interaction and perturbation mechanisms induced by two cationic cell penetrating peptides with distinct charge distribution
    Alves, Isabel D.
    Goasdoue, Nicole
    Correia, Isabelle
    Aubry, Soline
    Galanth, Cecile
    Sagan, Sandrine
    Lavielle, Solange
    Chassaing, Gerard
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (7-8): : 948 - 959
  • [3] [Anonymous], 1981, Phys. Des. defauts (Phys. Defects)
  • [4] Modulation of CTP:phosphocholine cytidylyltransferase by membrane curvature elastic stress
    Attard, GS
    Templer, RH
    Smith, WS
    Hunt, AN
    Jackowski, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) : 9032 - 9036
  • [5] Orientations of helical peptides in membrane bilayers by solid state NMR spectroscopy
    Bechinger, B
    Gierasch, LM
    Montal, M
    Zasloff, M
    Opella, SJ
    [J]. SOLID STATE NUCLEAR MAGNETIC RESONANCE, 1996, 7 (03) : 185 - 191
  • [6] Structure and dynamics of the antibiotic peptide PGLa in membranes by solution and solid-state nuclear magnetic resonance spectroscopy
    Bechinger, B
    Zasloff, M
    Opella, SJ
    [J]. BIOPHYSICAL JOURNAL, 1998, 74 (02) : 981 - 987
  • [7] Detergent-like actions of linear amphipathic cationic antimicrobial peptides
    Bechinger, Burkhard
    Lohner, Karl
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (09): : 1529 - 1539
  • [8] Rationalizing the membrane interactions of cationic amphipathic antimicrobial peptides by their molecular shape
    Bechinger, Burkhard
    [J]. CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2009, 14 (05) : 349 - 355
  • [9] Ben-Shaul A, 1995, HDB BIOL PHYS A&B, V1, P359
  • [10] Blondelle SE, 2010, CURR PHARM DESIGN, V16, P3204