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Nanoscale aggregation of cellular β_2-adrenergic receptors measured by plasmonic interactions of functionalized nanoparticles

机译:通过功能化的纳米粒子的等离子体相互作用测量细胞β_2-肾上腺素受体的纳米级聚集。

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摘要

Adrenergic signaling that controls the contraction of cardiac myocyte cells and the beating of the mammalian heart is initiated by ligand binding to adrenergic receptors contained in nanoscale multiprotein complexes at the cellular membrane. Here we demonstrate that the surface-enhanced Raman scattering (SERS) of functionalized silver nanoparticles can be used to report on the receptor aggregation state of specifically label β_2- adrenergic receptors on mouse cardiac myocyte cells. Furthermore, multimodal imaging including Raman, Rayleigh scattering, scanning electron microscopy, and luminescence imaging was combined to fully characterize the β_2- adrenergic receptor-mediated aggregation of silver nanoparticles on the membrane of cardiac myocytes. Scanning electron microscopy analysis reveals distinct SERS active clusters of between 10 and 70 nanoparticles per signaling domain from ultra-high-resolution images of β_2-adrenergic receptor clusters on the cellular membrane. These techniques can be generally applied to study the aggregation of other cell surface receptors and explore their distribution on cell surfaces.
机译:通过配体与细胞膜上纳米级多蛋白复合物中所含的肾上腺素能受体的结合,开始控制心肌细胞收缩和哺乳动物心脏跳动的肾上腺素能信号传导。在这里,我们证明功能化的银纳米粒子的表面增强拉曼散射(SERS)可用于报告小鼠心肌细胞上特异性标记β_2-肾上腺素能受体的受体聚集状态。此外,包括拉曼,瑞利散射,扫描电子显微镜和发光成像的多峰成像相结合,以充分表征心肌细胞膜上的银纳米粒子的β_2-肾上腺素能受体介导的聚集。扫描电子显微镜分析从细胞膜上的β_2-肾上腺素受体簇的超高分辨率图像中发现,每个信号域的SERS活性簇分别为10至70个纳米颗粒。这些技术通常可用于研究其他细胞表面受体的聚集并探索它们在细胞表面的分布。

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