Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, USA.
University of Washington, Department of Bioengineering, Seattle, WA, USA.
Methods Mol Biol. 2022;2475:61-77. doi: 10.1007/978-1-0716-2217-9_4.
Plasma membrane receptors are transmembrane proteins that initiate cellular response following the binding of specific ligands (e.g., growth factors, hormones, and cytokines). The abundance of plasma membrane receptors can be a diagnostic or prognostic biomarker in many human diseases. One of the best techniques for measuring plasma membrane receptors is quantitative flow cytometry (qFlow). qFlow employs fluorophore-conjugated antibodies against the receptors of interest and corresponding fluorophore-loaded calibration beads offers standardized and reproducible measurements of plasma membrane receptors. More importantly, qFlow can achieve absolute quantification of plasma membrane receptors when phycoerythrin (PE) is the fluorophore of choice. Here we describe a detailed qFlow protocol to obtain absolute receptor quantities on the basis of PE calibration. This protocol is foundational for many previous and ongoing studies in quantifying tyrosine kinase receptors and G-protein-coupled receptors with in vitro cell models and ex vivo cell samples.
质膜受体是一种跨膜蛋白,在与特定配体(如生长因子、激素和细胞因子)结合后,会引发细胞反应。在许多人类疾病中,质膜受体的丰度可以作为诊断或预后的生物标志物。测量质膜受体的最佳技术之一是定量流式细胞术(qFlow)。qFlow 使用针对感兴趣的受体的荧光素偶联抗体和相应的荧光素加载校准珠,提供标准化和可重复的质膜受体测量。更重要的是,当藻红蛋白(PE)是首选荧光染料时,qFlow 可以实现质膜受体的绝对定量。在这里,我们描述了一个详细的 qFlow 方案,该方案基于 PE 校准来获得绝对受体数量。该方案是以前和正在进行的许多研究的基础,这些研究使用体外细胞模型和体外细胞样本来定量酪氨酸激酶受体和 G 蛋白偶联受体。