Suppr超能文献

用于趋化因子受体信号传导的双色荧光素酶互补技术

Dual-Color Luciferase Complementation for Chemokine Receptor Signaling.

作者信息

Luker Kathryn E, Luker Gary D

机构信息

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.

出版信息

Methods Enzymol. 2016;570:119-29. doi: 10.1016/bs.mie.2015.08.024. Epub 2015 Nov 14.

Abstract

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.

摘要

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。

相似文献

1
Dual-Color Luciferase Complementation for Chemokine Receptor Signaling.
Methods Enzymol. 2016;570:119-29. doi: 10.1016/bs.mie.2015.08.024. Epub 2015 Nov 14.
2
Imaging ligand-dependent activation of CXCR7.
Neoplasia. 2009 Oct;11(10):1022-35. doi: 10.1593/neo.09724.
3
Bioluminescent CXCL12 fusion protein for cellular studies of CXCR4 and CXCR7.
Biotechniques. 2009 Jul;47(1):625-32. doi: 10.2144/000113126.
4
Split Gaussia luciferase for imaging ligand-receptor binding.
Methods Mol Biol. 2014;1098:59-69. doi: 10.1007/978-1-62703-718-1_5.
5
Allosteric peptide regulators of chemokine receptors CXCR4 and CXCR7.
Biochem Pharmacol. 2013 Nov 1;86(9):1263-71. doi: 10.1016/j.bcp.2013.08.019. Epub 2013 Aug 22.
6
Secreted CXCL12 (SDF-1) forms dimers under physiological conditions.
Biochem J. 2012 Mar 1;442(2):433-42. doi: 10.1042/BJ20111341.
7
Imaging CXCR4 signaling with firefly luciferase complementation.
Anal Chem. 2008 Jul 15;80(14):5565-73. doi: 10.1021/ac8005457. Epub 2008 Jun 6.
8
CXCR7 controls competition for recruitment of β-arrestin 2 in cells expressing both CXCR4 and CXCR7.
PLoS One. 2014 Jun 4;9(6):e98328. doi: 10.1371/journal.pone.0098328. eCollection 2014.
10
Imaging CXCL12-CXCR4 signaling in ovarian cancer therapy.
PLoS One. 2013;8(1):e51500. doi: 10.1371/journal.pone.0051500. Epub 2013 Jan 23.

本文引用的文献

1
CXCR7 controls competition for recruitment of β-arrestin 2 in cells expressing both CXCR4 and CXCR7.
PLoS One. 2014 Jun 4;9(6):e98328. doi: 10.1371/journal.pone.0098328. eCollection 2014.
2
Linkers in the structural biology of protein-protein interactions.
Protein Sci. 2013 Feb;22(2):153-67. doi: 10.1002/pro.2206. Epub 2013 Jan 8.
5
Luciferase protein complementation assays for bioluminescence imaging of cells and mice.
Methods Mol Biol. 2011;680:29-43. doi: 10.1007/978-1-60761-901-7_2.
6
Dual-color click beetle luciferase heteroprotein fragment complementation assays.
Chem Biol. 2010 Sep 24;17(9):1018-29. doi: 10.1016/j.chembiol.2010.06.018.
7
Beta-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7.
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):628-32. doi: 10.1073/pnas.0912852107. Epub 2009 Dec 17.
9
Imaging CXCR4 signaling with firefly luciferase complementation.
Anal Chem. 2008 Jul 15;80(14):5565-73. doi: 10.1021/ac8005457. Epub 2008 Jun 6.
10
A highly sensitive protein-protein interaction assay based on Gaussia luciferase.
Nat Methods. 2006 Dec;3(12):977-9. doi: 10.1038/nmeth979. Epub 2006 Nov 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验