| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10749675 | Biochemical and Biophysical Research Communications | 2016 | 6 Pages | 
Abstract
												Mutations in Prokineticin receptor 2 (PKR2), a G-protein-coupled receptor, have been identified in patients with Kallmann syndrome and/or idiopathic hypogonadotropic hypogonadism, characterized by delayed puberty and infertility. In this study, we performed yeast two-hybrid screening by using PKR2 C-terminus (amino acids 333-384) as a bait, and identified Snapin as a novel interaction partner for PKR2. The interaction of Snapin and PKR2 was confirmed in GST pull-down and co-immunoprecipitation studies. We further demonstrated that two α-helix domains in Snapin are required for the interaction. And the interactive motifs of PKR2 were mapped to YFK (343-345) and HWR (351-353), which shared a similar sequence of two aromatic amino acids followed by a basic amino acid. Disruption of Snapin-PKR2 interaction did not affect PKR2 signaling, but increased the ligand-induced degradation, implying a role of Snapin in the trafficking of PKR2.
											Keywords
												GFPGnRHSnapinProkineticin receptorPKR2IHHPKRGPCRsGSTG protein-coupled receptorsG-protein coupled receptorSodium dodecyl sulfatepolyacrylamide gel electrophoresisSDS-PAGEKallmann syndromeYeast two hybridGonadotropin-releasing hormoneidiopathic hypogonadotropic hypogonadismGreen fluorescence proteinProkineticinglutathione S-transferase
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											Authors
												Jian Song, Jie Li, Hua-die Liu, Wei Liu, Yong Feng, Xiao-Tao Zhou, Jia-Da Li, 
											