The impact of peptides on lipid membranes

被引:126
作者
Khandelia, Himanshu [1 ]
Ipsen, John H. [1 ]
Mouritsen, Ole G. [1 ]
机构
[1] Univ So Denmark, Dept Chem & Phys, MEMPHYS Ctr Biomembrane Phys, DK-5230 Odense M, Denmark
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2008年 / 1778卷 / 7-8期
关键词
lipid-bilayer membrane; antimicrobial peptide; acylation; prenylation; gramicidin A; molecular dynamics simulation;
D O I
10.1016/j.bbamem.2008.02.009
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
We review the fundamental strategies used by small peptides to associate with lipid membranes and how the different strategies impact on the structure and dynamics of the lipids. In particular we focus on the binding of amphiphilic peptides by electrostatic and hydrophobic forces, on the anchoring of peptides to the bilayer by acylation and prenylation, and on the incorporation of small peptides that form well-defined channels. The effect of lipid-peptide interactions on the lipids is characterized in terms of lipid acyl-chain order, membrane thickness, membrane elasticity, permeability, lipid-domain and annulus formation, as well as acyl-chain dynamics. The different situations are illustrated by specific cases for which experimental observations can be interpreted and supplemented by theoretical modeling and simulations. A comparison is made with the effect on lipids of trans-membrane proteins. The various cases are discussed in the context of the possible roles played by lipid-peptide interactions for the biological, physiological, and pharmacological function of peptides. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1528 / 1536
页数:9
相关论文
共 90 条
[71]   Farnesol-DMPC phase behaviour:: a 2H-NMR study [J].
Rowat, AC ;
Davis, JH .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1661 (02) :178-187
[72]   THE BIOPHYSICS OF PEPTIDE MODELS OF ION CHANNELS [J].
SANSOM, MSP .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1991, 55 (03) :139-235
[73]   Impact of single-residue mutations on the structure and function of ovispirin/novispirin antimicrobial peptides [J].
Sawai, MV ;
Waring, AJ ;
Kearney, WR ;
McCray, PB ;
Forsyth, WR ;
Lehrer, RI ;
Tack, BF .
PROTEIN ENGINEERING, 2002, 15 (03) :225-232
[74]   Mechanism of the binding, insertion and destabilization of phospholipid bilayer membranes by α-helical antimicrobial and cell non-selective membrane-lytic peptides [J].
Shai, Y .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1462 (1-2) :55-70
[75]   Interactions of the designed antimicrobial peptide MB21 and truncated dermaseptin S3 with lipid bilayers: molecular-dynamics simulations [J].
Shepherd, CM ;
Vogel, HJ ;
Tieleman, DP .
BIOCHEMICAL JOURNAL, 2003, 370 :233-243
[76]   FLUOROMETRIC EVALUATION OF THE AFFINITIES OF ISOPRENYLATED PEPTIDES FOR LIPID BILAYERS [J].
SILVIUS, JR ;
LHEUREUX, F .
BIOCHEMISTRY, 1994, 33 (10) :3014-3022
[77]   Mechanisms of Ras protein targeting in mammalian cells [J].
Silvius, JR .
JOURNAL OF MEMBRANE BIOLOGY, 2002, 190 (02) :83-92
[78]   Lipid modifications of intracellular signal-transducing proteins [J].
Silvius, JR .
JOURNAL OF LIPOSOME RESEARCH, 1999, 9 (01) :1-19
[79]   Position-dependent hydrophobicity of the antimicrobial magainin peptide affects the mode of peptide-lipid interactions and selective toxicity [J].
Tachi, T ;
Epand, RF ;
Epand, RM ;
Matsuzaki, K .
BIOCHEMISTRY, 2002, 41 (34) :10723-10731
[80]   Antimicrobial peptides: New candidates in the fight against bacterial infections [J].
Toke, O .
BIOPOLYMERS, 2005, 80 (06) :717-735