Peptide interactions with bacterial lipopolysaccharides

被引:45
|
作者
Schmidtchen, Artur [1 ]
Malmsten, Martin [2 ]
机构
[1] Lund Univ, Dept Clin Sci, Sect Dermatol & Venereol, SE-22184 Lund, Sweden
[2] Uppsala Univ, Dept Pharm, SE-75123 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Anti-endotoxic; Antimicrobial; Lipid A; Lipopolysaccharide; Peptide; HOST-DEFENSE PEPTIDES; C-TERMINAL PEPTIDES; ANTIMICROBIAL PEPTIDES; ENDOTOXIN NEUTRALIZATION; BIOPHYSICAL CHARACTERIZATION; BINDING; MEMBRANE; ACTIVATION; PROTEIN; CELLS;
D O I
10.1016/j.cocis.2013.06.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Peptide and protein interactions with (lipo)polysaccharides are important in various biological contexts, including lipoprotein deposition at proteoglycan-covered endothelial surfaces in atherosclerosis, lectin functionality, and the interaction of antimicrobial and anti-inflammatory peptides and proteins with (lipo)polysaccharides. The latter of these areas, which is the topic of this review, has attracted considerable interest during the last few years, since antimicrobial peptides may offer novel therapeutic opportunities in an era of growing problems with antibiotic resistance, and persisting problems with both acute and chronic inflammation. In the present overview, physicochemical factors affecting peptide interactions with bacterial (lipo)polysaccharides are discussed, both in solution and at membrane interfaces. In doing so, an attempt is made to illustrate how physicochemical factors affect the antimicrobial and anti-endotoxic functionality of such peptides, and how knowledge on this can be translated into therapeutic opportunities, e.g., in sepsis. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:381 / 392
页数:12
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