脂多糖结合蛋白
阳离子聚合
化学
脂多糖
抗菌肽
肽
抗菌剂
血浆蛋白结合
CD14型
生物化学
受体
生物
免疫学
有机化学
作者
Monisha G. Scott,Anita Vreugdenhil,Wim A. Buurman,Robert E. W. Hancock,Michael R. Gold
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2000-01-15
卷期号:164 (2): 549-553
被引量:276
标识
DOI:10.4049/jimmunol.164.2.549
摘要
Abstract We investigated the mechanism by which cationic antimicrobial peptides block the activation of macrophages by LPS. The initial step in LPS signaling is the transfer of LPS to CD14 by LPS binding protein (LBP). Because many cationic antimicrobial peptides bind LPS, we asked whether these peptides block the binding of LPS to LBP. Using an assay that measures the binding of LPS to immobilized LBP, we show for the first time that a variety of structurally diverse cationic antimicrobial peptides block the interaction of LPS with LBP. The relative ability of different cationic peptides to block the binding of LPS to LBP correlated with their ability to block LPS-induced TNF-α production by the RAW 264.7 macrophage cell line.
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