Solution Conformation of Nociceptin
Nociceptin, a novel heptadecapeptide, interacts with ORL1a G protein-coupled receptor whose sequence is closely related to that of the κ opioid receptor but has no opioid activity. We have investigated the conformational preferences of Nociceptin also in comparison to Dynorphin A. The N-terminal par...
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Veröffentlicht in: | Biochemical and biophysical research communications 1997-04, Vol.233 (3), p.640-643 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Nociceptin, a novel heptadecapeptide, interacts with ORL1a G protein-coupled receptor whose sequence is closely related to that of the κ opioid receptor but has no opioid activity. We have investigated the conformational preferences of Nociceptin also in comparison to Dynorphin A. The N-terminal part of Nociceptin has the same conformational preferences of the message of endogenous opioids but the C-terminal part of the sequence is more flexible than the corresponding address of Dynorphin A. [Tyr1]-Nociceptin, while retaining nociceptive activity, has also an opioid activity comparable to that of enkephalins. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1006/bbrc.1997.6285 |