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首页> 外文期刊>Chemphyschem: A European journal of chemical physics and physical chemistry >Receptor–Ligand Interactions: Binding Affinities Studied by Single-Molecule and Super-Resolution Microscopy on Intact Cells
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Receptor–Ligand Interactions: Binding Affinities Studied by Single-Molecule and Super-Resolution Microscopy on Intact Cells

机译:受体-配体相互作用:结合亲和力通过完整细胞上的单分子和超分辨率显微镜研究。

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摘要

Protein–ligand interactions play an important role in many biological processes. Notably, membrane receptors are the starting point for a huge variety of cellular signal transduction pathways. Quantifying the binding affinity of a ligand for its transmembrane receptor is of great importance as it provides information on the potency of the ligand. We developed a new experimental procedure to determine binding affinities of ligands for their membrane receptors directly on intact single cells using super-resolution imaging. Dissociation constants were determined by titrating fluorophore-labelled ligand against cells expressing the target protein and applying single-molecule imaging.
机译:蛋白质-配体相互作用在许多生物学过程中起着重要作用。值得注意的是,膜受体是多种细胞信号转导途径的起点。定量配体对其跨膜受体的结合亲和力非常重要,因为它提供了有关配体效能的信息。我们开发了一种新的实验程序,可以使用超分辨率成像直接确定完整的单个细胞上配体与其膜受体的结合亲和力。通过针对表达目标蛋白的细胞滴定荧光团标记的配体并应用单分子成像来确定解离常数。

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