Identification and molecular docking studies for novel inverse agonists of SREB, super conserved receptor expressed in brain. (17th May 2016)
- Record Type:
- Journal Article
- Title:
- Identification and molecular docking studies for novel inverse agonists of SREB, super conserved receptor expressed in brain. (17th May 2016)
- Main Title:
- Identification and molecular docking studies for novel inverse agonists of SREB, super conserved receptor expressed in brain
- Authors:
- Yanai, Toshihiro
Kurosawa, Aya
Nikaido, Yoshiaki
Nakajima, Nozomi
Saito, Tamio
Osada, Hiroyuki
Konno, Ayumu
Hirai, Hirokazu
Takeda, Shigeki - Abstract:
- Abstract : The identification of novel synthetic ligands for G protein‐coupled receptors (GPCRs) is important not only for understanding human physiology, but also for the development of novel drugs, especially for orphan GPCRs for which endogenous ligands are unknown. One of the orphan GPCR subfamilies, Super conserved Receptor Expressed in Brain (SREB), consists of GPR27, GPR85 and GPR173 and is expressed in the central nervous system. We report herein the identification of inverse agonists for the SREB family without their agonists. We carried out an in vitro screening of 5472 chemical compounds from the RIKEN NPDepo chemical library. The binding of [ 35 S]GTPγS to the GPR173–Gsα fusion protein expressed in Sf9 cells was measured and resulted in the identification of 8 novel GPR173 inverse agonists. The most potent compound showed an IC50 of approximately 8 μm . The identified compounds were also antagonists for other SREB members, GPR27 and GPR85. These results indicated that the SREB family could couple Gs‐type G proteins, and SREB–Gsα fusion proteins showed significant constitutive activities. Moreover, a molecular model of GPR173 was constructed using the screening results. The combination of computational and biological methods will provide a unique approach to ligand identification for orphan GPCRs and brain research. Abstract : One of the orphan GPCR subfamilies, Super conserved Receptor Expressed in Brain (SREB), consists of GPR27, GPR85 and GPR173 and isAbstract : The identification of novel synthetic ligands for G protein‐coupled receptors (GPCRs) is important not only for understanding human physiology, but also for the development of novel drugs, especially for orphan GPCRs for which endogenous ligands are unknown. One of the orphan GPCR subfamilies, Super conserved Receptor Expressed in Brain (SREB), consists of GPR27, GPR85 and GPR173 and is expressed in the central nervous system. We report herein the identification of inverse agonists for the SREB family without their agonists. We carried out an in vitro screening of 5472 chemical compounds from the RIKEN NPDepo chemical library. The binding of [ 35 S]GTPγS to the GPR173–Gsα fusion protein expressed in Sf9 cells was measured and resulted in the identification of 8 novel GPR173 inverse agonists. The most potent compound showed an IC50 of approximately 8 μm . The identified compounds were also antagonists for other SREB members, GPR27 and GPR85. These results indicated that the SREB family could couple Gs‐type G proteins, and SREB–Gsα fusion proteins showed significant constitutive activities. Moreover, a molecular model of GPR173 was constructed using the screening results. The combination of computational and biological methods will provide a unique approach to ligand identification for orphan GPCRs and brain research. Abstract : One of the orphan GPCR subfamilies, Super conserved Receptor Expressed in Brain (SREB), consists of GPR27, GPR85 and GPR173 and is expressed in the central nervous system. We report the identification of inverse agonists for the SREB family without their agonists. … (more)
- Is Part Of:
- Genes to cells. Volume 21:Number 7(2016)
- Journal:
- Genes to cells
- Issue:
- Volume 21:Number 7(2016)
- Issue Display:
- Volume 21, Issue 7 (2016)
- Year:
- 2016
- Volume:
- 21
- Issue:
- 7
- Issue Sort Value:
- 2016-0021-0007-0000
- Page Start:
- 717
- Page End:
- 727
- Publication Date:
- 2016-05-17
- Subjects:
- Cytogenetics -- Periodicals
Cells -- Mechanical properties -- Periodicals
Molecular genetics -- Periodicals
Genes -- Periodicals
Molecular biology -- Periodicals
Cytology -- Periodicals
Biomechanics -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2443 ↗
http://www.blacksci.co.uk/%7Ecgilib/jnlpage.bin?Journal=GTC&File=GTC&Page=aims ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/gtc.12378 ↗
- Languages:
- English
- ISSNs:
- 1356-9597
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4111.762500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2219.xml