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Structure of the agonist-bound neurotensin receptor

Authors :
White, Jim F.
Noinaj, Nicholas
Shibata, Yoko
Love, James
Kloss, Brian
Xu, Feng
Gvozdenovic-Jeremic, Jelena
Shah, Priyanka
Shiloach, Joseph
Tate, Christopher G.
Grisshammer, Reinhard
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