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Microscopic Visualization of Metabotropic GlutamateReceptors on the Surface of Living Cells Using Bifunctional MagneticResonance Imaging Probes

机译:代谢型谷氨酸的显微可视化使用双功能磁性的活细胞表面上的受体共振成像探头

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摘要

A series of bimodal metabotropic glutamate-receptor targeted MRI contrast agents has been developed and evaluated, based on established competitive metabotropic Glu receptor subtype 5 (mGluR5) antagonists. In order to directly visualize mGluR5 binding of these agents on the surface of live astrocytes, variations in the core structure were made. A set of gadolinium conjugates containing either a cyanine dye or a fluorescein moiety was accordingly prepared, to allow visualization by optical microscopy in cellulo. In each case, surface receptor binding was compromised and cell internalization observed. Another approach, examining the location of a terbium analogue via sensitized emission, also exhibited nonspecific cell uptake in neuronal cell line models. Finally, biotin derivatives of two lead compounds were prepared, and the specificity of binding to the mGluR5 cell surface receptors was demonstrated with the aid of their fluorescently labeled avidin conjugates, using both total internal reflection fluorescence (TIRF) and confocal microscopy.
机译:基于已建立的竞争性代谢型Glu受体亚型5(mGluR5)拮抗剂,已开发和评估了一系列针对双峰代谢型谷氨酸受体的MRI造影剂。为了直接可视化这些试剂在活的星形胶质细胞表面上的mGluR5结合,对核心结构进行了变异。相应地制备了一组包含花青染料或荧光素部分的conjugate共轭物,以允许在纤维素中通过光学显微镜观察。在每种情况下,表面受体结合均受到损害,并观察到细胞内在化。通过敏化发射检查emission类似物的位置的另一种方法在神经元细胞系模型中也表现出非特异性细胞摄取。最后,制备了两种先导化合物的生物素衍生物,并使用全内反射荧光(TIRF)和共聚焦显微镜,借助其荧光标记的抗生物素蛋白结合物证明了与mGluR5细胞表面受体结合的特异性。

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