Centre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
Centre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
Trends Pharmacol Sci. 2018 Feb;39(2):175-186. doi: 10.1016/j.tips.2017.09.001. Epub 2017 Oct 9.
Spatial intensity distribution analysis (SpIDA) is a recently developed approach for determining quaternary structure information on fluorophore-labelled proteins of interest in situ. It can be applied to live or fixed cells and native tissue. Using confocal images, SpIDA generates fluorescence intensity histograms that are analysed by super-Poissonian distribution functions to obtain density and quantal brightness values of the fluorophore-labelled protein of interest. This allows both expression level and oligomerisation state of the protein to be determined. We describe the application of SpIDA to investigate the oligomeric state of G protein-coupled receptors (GPCRs) at steady state and following cellular challenge, and consider how SpIDA may be used to explore GPCR quaternary organisation in pathophysiology and to stratify medicines.
空间强度分布分析(SpIDA)是一种最近开发的方法,用于确定荧光标记的感兴趣蛋白质的四级结构信息原位。它可应用于活细胞或固定细胞和天然组织。使用共聚焦图像,SpIDA 生成荧光强度直方图,然后通过超泊松分布函数进行分析,以获得荧光标记的感兴趣蛋白质的密度和量子亮度值。这允许确定蛋白质的表达水平和寡聚状态。我们描述了 SpIDA 在研究稳态和细胞刺激后 G 蛋白偶联受体(GPCR)的寡聚状态中的应用,并考虑了 SpIDA 如何用于探索病理生理学中的 GPCR 四级组织和分层药物。