Mode of action of membrane active antimicrobial peptides

被引:1326
作者
Shai, Y [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
关键词
lytic peptides; antimicrobial peptides; antibacterial peptides; peptide-lipid interaction; diasteromeric cationic peptides;
D O I
10.1002/bip.10260
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
Water membrane soluble protein and peptide toxins are used m the defense and offense systems of all organisms, including plants and humans. A major group includes antimicrobial peptides, which serve as a nonspecific defense system that complements the highly specific cell-mediated immune response. The increasing resistance of bacteria to conventional antibiotics stimulated the isolation and characterization of many antimicrobial peptides for potential use as new target antibiotics. The finding of thousands of antimicrobial peptides with variable lengths and sequences, all of which are active at similar concentrations, suggests a general mechanism for killing bacteria rather than a specific mechanism that requires preferred active structures. Such a mechanism is in agreement with the "carpet model" that does not require any specific structure or sequence. It seems that when there is an appropriate balance between hydrophobicity and a net positive charge the peptides are active an bacteria. However, selective activity depends also on other parameters, such as the volume of the molecule, its structure, and its oligomeric state in solution and membranes. Further, although many studies support that bacterial membrane damage is a lethal event for bacteria, other studies point to a multihit mechanism in which the peptide binds to several targets in the cytoplasmic region of the bacteria. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:236 / 248
页数:13
相关论文
共 121 条
[21]  
2-#
[22]   ANTIMICROBIAL PEPTIDE MAGAININ-I FROM XENOPUS SKIN FORMS ANION-PERMEABLE CHANNELS IN PLANAR LIPID BILAYERS [J].
DUCLOHIER, H ;
MOLLE, G ;
SPACH, G .
BIOPHYSICAL JOURNAL, 1989, 56 (05) :1017-1021
[23]   ELECTRICALLY GATED IONIC CHANNELS IN LIPID BILAYERS [J].
EHRENSTEIN, G ;
LECAR, H .
QUARTERLY REVIEWS OF BIOPHYSICS, 1977, 10 (01) :1-34
[24]   Diversity of antimicrobial peptides and their mechanisms of action [J].
Epand, RM ;
Vogel, HJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1462 (1-2) :11-28
[25]   Antibacterial agents based on the cyclic D,L-α-peptide architecture [J].
Fernandez-Lopez, S ;
Kim, HS ;
Choi, EC ;
Delgado, M ;
Granja, JR ;
Khasanov, A ;
Kraehenbuehl, K ;
Long, G ;
Weinberger, DA ;
Wilcoxen, KM ;
Ghadiri, MR .
NATURE, 2001, 412 (6845) :452-455
[26]   Covalent structure, synthesis, and structure-function studies of mesentericin Y 105(37), a defensive peptide from gram-positive bacteria Leuconostoc mesenteroides [J].
Fleury, Y ;
Dayem, MA ;
Montagne, JJ ;
Chaboisseau, E ;
LeCaer, JP ;
Nicolas, P ;
Delfour, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :14421-14429
[27]   THE ALPHA-5 SEGMENT OF BACILLUS-THURINGIENSIS DELTA-ENDOTOXIN - IN-VITRO ACTIVITY, ION-CHANNEL FORMATION AND MOLECULAR MODELING [J].
GAZIT, E ;
BACH, D ;
KERR, ID ;
SANSOM, MSP ;
CHEJANOVSKY, N ;
SHAI, Y .
BIOCHEMICAL JOURNAL, 1994, 304 :895-902
[28]   STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF THE ALPHA-5 SEGMENT OF BACILLUS-THURINGIENSIS DELTA-ENDOTOXIN [J].
GAZIT, E ;
SHAI, Y .
BIOCHEMISTRY, 1993, 32 (13) :3429-3436
[29]   Structure and orientation of the mammalian antibacterial peptide cecropin P1 within phospholipid membranes [J].
Gazit, E ;
Miller, IR ;
Biggin, PC ;
Sansom, MSP ;
Shai, Y .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 258 (05) :860-870
[30]   MODE OF ACTION OF THE ANTIBACTERIAL CECROPIN B2 - A SPECTROFLUOROMETRIC STUDY [J].
GAZIT, E ;
LEE, WJ ;
BREY, PT ;
SHAI, YC .
BIOCHEMISTRY, 1994, 33 (35) :10681-10692