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BRET技术在G蛋白偶联受体与β-arrestins相互作用研究中的应用进展 被引量:3

Application of BRET technology in interaction of G protein-coupled receptor with β-arrestins:recent progress
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摘要 G蛋白偶联受体(G protein-coupled receptor,GPCR)是一个重要的细胞膜受体超家族。β-arrestin 1和β-ar-restin 2是广泛存在于细胞内的调配器和支架蛋白,它们在G蛋白偶联受体的细胞内信号转导、脱敏、内化、复敏以及G蛋白非依赖的信号转导中发挥重要作用。生物发光共振能量转移(BRET)技术能够实时监测活细胞内GPCRs和β-arrestins的相互作用,可进一步阐明β-arrestin调节GPCRs的作用机制,有助于开发新一代影响GPCRs功能活动的药物。 G protein-coupled receptors constitute an important super family of cell surface proteins.β-arrestin 1and 2 are widely expressed intracellular adaptor and scaffolding proteins playing important roles in G protein-coupled receptor desensitization,internalization,intracellular trafficking,and G protein-independent signaling.Recent development in bioluminescence resonance energy transfer(BRET)technology makes it possible to monitor the GPCR-β-arrestin complexes in live cells in a real-time manner;and investigators can further elucidate the ever-expanding roles ofβ-arrestins in mediating GPCR function,which will help to develop the new generation of drugs targeting GPCRs
出处 《第二军医大学学报》 CAS CSCD 北大核心 2011年第10期1140-1143,共4页 Academic Journal of Second Military Medical University
基金 国家自然科学基金(30870932 30971081) 山东省自然科学基金(ZR2009D2004)~~
关键词 Β-ARRESTIN G蛋白偶联受体 信号转导 生物发光共振能量转移 β-arrestin G protein-coupled receptor signal transduction bioluminescence resonance energy transfer
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  • 1Tatemoto K, Hosoya M, Habata Y, Fujii R, Kakegawa T, Zou MX, Kawamata Yet al. Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor. Biochem Biophys Res Commun 1998, 251:471-476 被引量:1
  • 2Habata Y, Fujii R, Hosoya M, Fukusumi S, Kawamata Y, Hinuma S, Kitada C et al. Apelin, the natural ligand of the orphan receptor APJ, is abundantly secreted in the colostrum. Biochim Biophys Acta 1999, 1452:25-35 被引量:1
  • 3Reaux A, De Mota N, Skultetyova I, Lenkei Z, E1 Messari S, Gallatz K, Corvol Pet al. Physiological role of a novel neuropeptide, apelin, and its receptor in the rat brain. J Neurochem 2001, 77: 1085-1096 被引量:1
  • 4Wang G, Anini Y, Wei W, Qi X, OCarroll AM, Mochizuki T, Wang HQ et al. Apelin, a new enteric peptide: localization in the gastrointestinal tract, ontogeny, and stimulation of gastric cell proliferation and of cholecystokinin secretion. Endocrinology 2004, 145:1342-1348 被引量:1
  • 5Lee DK, Cheng R, Nguyen T, Fan T, Kariyawasam AP, Liu Y, Osmond DH et al. Characterization of apelin, the ligand for the APJ receptor. J Neurochem 2000, 74:34-41 被引量:1
  • 6Boucher J, Masri B, Daviaud D, Gesta S, Guigne C, Mazzucotelli A, Castan-Laurell I et al. Apelin, a newly identified adipokine upregulated by insulin and obesity. Endocrinology 2005, 146: 17641771 被引量:1
  • 7Kleinz M J, Davenport AP. Emerging roles of apelin in biology and medicine. Pharmacol Ther 2005, 107:198-211 被引量:1
  • 8Sunter D, Hewson AK, Dickson SL. Intracerebroventricular injection of apelin-13 reduces food intake in the rat. Neurosci Lett 2003, 353:1-4 被引量:1
  • 9Szokodi I, Tavi E Foldes G, Voutilainen-Myllyla S, Ilves M, Tokola H, Pikkarainen Set al. Apelin, the novel endogenous ligand of the orphan receptor APJ, regulates cardiac contractility. Circ Res 2002, 91:434-440 被引量:1
  • 10Horiuchi Y, Fujii T, Kamimura Y, Kawashima K. The endogenous, immunologically active peptide apelin inhibits lymphocytic cholinergic activity during immunological responses. J Neuroimmunol 2003, 144:46-52 被引量:1

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