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
Hauptverfasser: Motoyama, Shihoko, Takada, Kiyoshi, Yasunaga, Teruo, Fujita, Tsugumi, Shimohigashi, Yasuyuki
Format: Artikel
Sprache:eng
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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.
ISSN:0009-2673
1348-0634