Luker Kathryn E, Luker Gary D
Department of Radiology, Center for Molecular Imaging, University of Michigan, Ann Arbor, Michigan, USA.
Department of Radiology, Center for Molecular Imaging, University of Michigan, Ann Arbor, Michigan, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA; Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Methods Enzymol. 2016;570:119-29. doi: 10.1016/bs.mie.2015.08.024. Epub 2015 Nov 14.
Chemokine receptors may share common ligands, setting up potential competition for ligand binding, and association of activated receptors with downstream signaling molecules such as β-arrestin. Determining the "winner" of competition for shared effector molecules is essential for understanding integrated functions of chemokine receptor signaling in normal physiology, disease, and response to therapy. We describe a dual-color click beetle luciferase complementation assay for cell-based analysis of interactions of two different chemokine receptors, CXCR4 and ACKR3, with the intracellular scaffolding protein β-arrestin 2. This assay provides real-time quantification of receptor activation and signaling in response to chemokine CXCL12. More broadly, this general imaging strategy can be applied to quantify interactions of any set of two proteins that interact with a common binding partner.
趋化因子受体可能共享共同的配体,从而引发配体结合的潜在竞争,以及活化受体与下游信号分子(如β-抑制蛋白)的关联。确定共享效应分子竞争的“胜者”对于理解趋化因子受体信号在正常生理、疾病及治疗反应中的综合功能至关重要。我们描述了一种基于细胞的双色叩甲荧光素酶互补分析方法,用于分析两种不同趋化因子受体CXCR4和ACKR3与细胞内支架蛋白β-抑制蛋白2的相互作用。该分析方法可实时定量趋化因子CXCL12诱导的受体激活和信号传导。更广泛地说,这种通用的成像策略可用于定量任何一组与共同结合伴侣相互作用的两种蛋白质之间的相互作用。