1. Academic Validation
  2. Structure of the agonist-bound neurotensin receptor

Structure of the agonist-bound neurotensin receptor

  • Nature. 2012 Oct 25;490(7421):508-13. doi: 10.1038/nature11558.
Jim F White 1 Nicholas Noinaj Yoko Shibata James Love Brian Kloss Feng Xu Jelena Gvozdenovic-Jeremic Priyanka Shah Joseph Shiloach Christopher G Tate Reinhard Grisshammer
Affiliations

Affiliation

  • 1 Membrane Protein Structure Function Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Department of Health and Human Services, Rockville, Maryland 20852, USA.
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(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.

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