targeted ubiquitination and degradation of g-protein-coupled receptor kinase 5 by the ddb1-cul4 ubiquitin ligase complex有针对性的泛素化和退化ddb1-cul4 g-protein-coupled受体激酶5的泛素连接酶复杂.pdfVIP

Targeted Ubiquitination and Degradation of G-Protein- Coupled Receptor Kinase 5 by the DDB1-CUL4 Ubiquitin Ligase Complex Ziyan Wu, Yuejun Chen*, Tong Yang, Qinqin Gao, Man Yuan, Lan Ma The State Key Laboratory of Medical Neurobiology and Pharmacology Research Center, Shanghai Medical College and Institutes of Brain Science, Fudan University, Shanghai, China Abstract The G protein-coupled receptor kinases (GRKs) phosphorylate agonist occupied G protein-coupled receptors (GPCRs) and desensitize GPCR-mediated signaling. Recent studies indicate they also function non-catalytically via interaction with other proteins. In this study, a proteomic approach was used to screen interacting proteins of GRK5 in MDA-MB-231 cells and HUVEC cells. Mass spectrometry analysis reveals several proteins in the GRK5 immunocomplex including damaged DNA- binding protein 1 (DDB1), an adaptor subunit of the CUL4-ROC1 E3 ubiquitin ligase complex. Co-immunoprecipitation experiments confirmed the association of GRK5 with DDB1-CUL4 complex, and reveal that DDB1 acts as an adapter to link GRK5 to CUL4 to form the complex. Overexpression of DDB1 promoted, whereas knockdown of DDB1 inhibited the ubiquitination of GRK5, and the degradation of GRK5 was reduced in cells deficient of DDB1. Furthermore, the depletion of DDB1 decreased Hsp90 inhibitor-induced GRK5 destabilization and UV irradiation-induced GRK5 degradation. Thus, our study identified potential GRK5 interacting proteins, and reveals the association of GRK5 with DDB1 in cell and the regulation of GRK5 level by DDB1-CUL4 ubiquitin ligase complex–dependent proteolysis pathway. Citation: Wu Z, Chen Y, Yang T, Gao Q, Yuan M, et al. (2012) Targeted Ubiquitination and Degradation of G-Protein-Coupled Receptor Kinase 5 by the DDB1-CUL4 Ubiquitin Ligase Complex. PLoS ONE 7(8): e43997.