首页> 外文会议>Conference on Single Molecule Spectroscopy and Imaging; 20080119-21; San Jose,CA(US) >Imaging of G protein-coupled receptors in solid-supported planar membranes at the single molecule level
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Imaging of G protein-coupled receptors in solid-supported planar membranes at the single molecule level

机译:固体支持平面膜中单分子水平的G蛋白偶联受体成像

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Odorant receptors are an excellent example of natural superiority in specifically binding specific, small and hydropho-bic molecules. They are of particular interest in the development of a sensor platform for G protein-coupled receptors (GPCRs). Odorant receptors (OR5) of Rattus norvegicus were incorporated into model membranes by in vitro synthesis and vectorial incorporation for achieving natural receptor function. The vectorial insertion of OR5 into the planar membrane and their lateral distribution, their interactions and their mobility within the membrane are of great importance for ligand-receptor interaction. We applied total internal reflection fluorescence (TIRF) microscopy and image analysis to assess the insertion and the OR5 distribution as well as the lateral mobility of these receptors at the single molecule level. The vectorial incorporation of OR5 into planar lipid membranes was investigated with TIRF microscopy and image segmentation. With increasing expression time, the OR5 incorporation density and aggregation increased linearly by about 0.02μm~(-2)min~(-1). The expression and incorporations of single OR5s were completed within about 8 minutes. The mobility of the incorporated receptors was measured with fluorescence correlation spectroscopy (FCS) and fluorescence recovery after photo-bleaching (FRAP). These measurements revealed that the incorporated receptors were immobilized with this class of lipid membranes.
机译:气味受体是特异性结合特定的,小的和疏水性分子的天然优势的一个很好的例子。在开发用于G蛋白偶联受体(GPCR)的传感器平台时,他们特别感兴趣。通过体外合成和载体掺入将褐家鼠的气味受体(OR5)掺入模型膜中,以实现天然受体功能。 OR5在平面膜中的矢量插入及其横向分布,它们之间的相互作用及其在膜内的迁移性对于配体-受体相互作用至关重要。我们应用了全内反射荧光(TIRF)显微镜和图像分析来评估在单个分子水平上这些受体的插入和OR5分布以及横向移动性。用TIRF显微镜和图像分割研究了OR5在平面脂质膜中的矢量掺入。随着表达时间的增加,OR5的掺入密度和聚集度线性增加约0.02μm〜(-2)min〜(-1)。单个OR5的表达和掺入在约8分钟内完成。通过荧光相关光谱法(FCS)和光漂白后的荧光恢复(FRAP)测量掺入受体的迁移率。这些测量结果表明,掺入的受体被这类脂质膜固定。

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