Exclusive Affinity-Labeling of [mu] Opioid Receptors by Morphiceptin Analogs Containing S-(3-Nitro-2-pyridylthio)cysteine
The S-(3-nitro-2-pyridylthio) (Npys) group only reacts with a free mercapto group to form a disulfide bond. A series of morphiceptin analogs containing SNpys-cysteine were designed and synthesized for specific affinity-labeling of μ opioid receptors. Affinity-labeling of opioid receptors was monitor...
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Veröffentlicht in: | Bulletin of the Chemical Society of Japan 1996-12, Vol.69 (12), p.3607 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The S-(3-nitro-2-pyridylthio) (Npys) group only reacts with a free mercapto group to form a disulfide bond. A series of morphiceptin analogs containing SNpys-cysteine were designed and synthesized for specific affinity-labeling of μ opioid receptors. Affinity-labeling of opioid receptors was monitored and evaluated by radioligand receptor binding assays using rat brain membranes and specific tritium-labeled ligands of enkephalin analogs. It was found that analogs with Cys(Npys) at position 4 or 5 bind covalently to μ receptors, but not to δ receptors, resulting in a discriminative and exclusive affinity labeling of μ opioid receptor subtype. |
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ISSN: | 0009-2673 1348-0634 |