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-Structure paper
タイトル | Molecular insights into the regulation of constitutive activity by RNA editing of 5HT serotonin receptors. |
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ジャーナル・号・ページ | Cell Rep, Vol. 40, Issue 7, Page 111211, Year 2022 |
掲載日 | 2022年8月16日 |
著者 | Ryan H Gumpper / Jonathan F Fay / Bryan L Roth / |
PubMed 要旨 | RNA editing is a process by which post-transcriptional changes of mRNA nucleotides alter protein function through modification of the amino acid content. The 5HT serotonin receptor, which undergoes ...RNA editing is a process by which post-transcriptional changes of mRNA nucleotides alter protein function through modification of the amino acid content. The 5HT serotonin receptor, which undergoes 32 distinct RNA-editing events leading to 24 protein isoforms, is a notable example of this process. These 5HT isoforms display differences in constitutive activity, agonist/inverse agonist potencies, and efficacies. To elucidate the molecular mechanisms responsible for these effects of RNA editing, we present four active-state 5HT-transducer-coupled structures of three representative isoforms (INI, VGV, and VSV) with the selective drug lorcaserin (Belviq) and the classic psychedelic psilocin. We also provide a comprehensive analysis of agonist activation and constitutive activity across all 24 protein isoforms. Collectively, these findings reveal a unique hydrogen-bonding network located on intracellular loop 2 that is subject to RNA editing, which differentially affects GPCR constitutive and agonist signaling activities. |
リンク | Cell Rep / PubMed:35977511 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.84 - 3.6 Å |
構造データ | EMDB-27633, PDB-8dpf: EMDB-27634, PDB-8dpg: EMDB-27635, PDB-8dph: EMDB-27636, PDB-8dpi: |
化合物 | ChemComp-T4U: ChemComp-CLR: ChemComp-91Q: |
由来 |
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キーワード | MEMBRANE PROTEIN / GPCR |