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Structure of the agonist-bound neurotensin receptor
- Source :
- Nature. October 25, 2012, Vol. 490 Issue 7421, p508, 8 p.
- Publication Year :
- 2012
-
Abstract
- Neurotensin (NTS) is a 13-amino-acid peptide that functions as both a neurotransmitter and a hormone through the activation of the neurotensin receptor NTSR1, a G-protein-coupled receptor (GPCR). In the brain, NTS modulates the activity of dopaminergic systems, opioid-independent analgesia, and the inhibition of food intake; in the gut, NTS regulates a range of digestive processes. Here we present the structure at 2.8 Å resolution of Rattus norvegicus NTSR1 in an active-like state, bound to [NTS.sub.8-13], the carboxy-terminal portion of NTS responsible for agonist-induced activation of the receptor. The peptide agonist binds to NTSR1 in an extended conformation nearly perpendicular to the membrane plane, with the C terminus oriented towards the receptor core. Our findings provide, to our knowledge, the first insight into the binding mode of a peptide agonist to a GPCR and may support the development of non-peptide ligands that could be useful in the treatment of neurological disorders, cancer and obesity.<br />Neurotensin (NTS) is a short peptide that is found in the nervous system and in peripheral tissues (1). NTS shows a wide range of biological activities and has important roles [...]
Details
- Language :
- English
- ISSN :
- 00280836
- Volume :
- 490
- Issue :
- 7421
- Database :
- Gale General OneFile
- Journal :
- Nature
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.306757687
- Full Text :
- https://doi.org/10.1038/nature11558