Suppr超能文献

荧光白三烯B4:潜在应用

Fluorescent leukotriene B4: potential applications.

作者信息

Sabirsh Alan, Wetterholm Anders, Bristulf Jesper, Leffler Hakon, Haeggström Jesper Z, Owman Christer

机构信息

Department of Medical Biochemistry and Biophysics, Division of Physiological Chemistry II, Karolinska Institute, Stockholm, Sweden.

出版信息

J Lipid Res. 2005 Jun;46(6):1339-46. doi: 10.1194/jlr.D500005-JLR200. Epub 2005 Apr 1.

Abstract

Leukotriene B4 (LTB4) is a potent lipid mediator of inflammation that acts primarily via a seven-transmembrane-spanning, G-protein-coupled receptor denoted BLT1. Here, we describe the synthesis and characterization of fluorescent analogs of LTB4 that are easy to produce, inexpensive, and without the disadvantages of a radioligand. Fluorescent LTB4 is useful for labeling LTB4 receptors for which no antibodies are available and for performing one-step fluorescence polarization assays conducive to high-throughput screening. We found that orange and green fluorescent LTB4 were full agonists that activated the LTB4 receptor BLT1 with EC50 values of 68 and 40 nM, respectively (4.5 nM for unmodified LTB4). Flow cytometric measurements and confocal imaging showed that fluorescent LTB4 colocalized with BLT1. Fluorescence polarization measurements showed that orange fluorescent LTB4 bound to BLT1 with a Kd of 66 nM and that this binding could be displaced by unlabeled LTB4 and other BLT1-specific ligands. Fluorescent LTB4 analogs were also able to displace tritiated LTB4. Orange fluorescent LTB4 binding to enhanced green fluorescent protein-tagged BLT1 could be observed using fluorescence resonance energy transfer. In addition to being a useful alternative to radiolabeled LTB4, the unique properties of fluorescently labeled LTB4 allow a variety of detection technologies to be used.

摘要

白三烯B4(LTB4)是一种强效的炎症脂质介质,主要通过一种七跨膜的G蛋白偶联受体(称为BLT1)发挥作用。在此,我们描述了LTB4荧光类似物的合成与表征,这些类似物易于制备、成本低廉,且没有放射性配体的缺点。荧光LTB4可用于标记没有可用抗体的LTB4受体,并用于进行有助于高通量筛选的一步荧光偏振分析。我们发现橙色和绿色荧光LTB4是完全激动剂,分别以68 nM和40 nM的EC50值激活LTB4受体BLT1(未修饰的LTB4为4.5 nM)。流式细胞术测量和共聚焦成像显示荧光LTB4与BLT1共定位。荧光偏振测量表明橙色荧光LTB4与BLT1结合的解离常数(Kd)为66 nM,且这种结合可被未标记的LTB4和其他BLT1特异性配体取代。荧光LTB4类似物也能够取代氚标记的LTB4。使用荧光共振能量转移可以观察到橙色荧光LTB4与增强型绿色荧光蛋白标记的BLT1的结合。除了作为放射性标记LTB4的有用替代品外,荧光标记LTB4的独特性质还允许使用多种检测技术。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验