Fukuda K, Kato S, Mori K
Department of Anesthesia, Kyoto University Hospital, Japan.
J Biol Chem. 1995 Mar 24;270(12):6702-9. doi: 10.1074/jbc.270.12.6702.
To elucidate which portions of the opioid receptor molecules are involved in the ligand selectivity, we have expressed chimeric receptors between the rat delta- and mu-opioid receptors from cDNAs and analysed their ligand binding properties. We demonstrate that the major binding determinant for the delta-selective enkephalin-related peptide, [D-Pen2,D-Pen5]enkephalin, resides within the region comprising the transmembrane segments V-VII and the intervening loop regions. On the other hand, the region spanning from the intracellular loop I to the amino-terminal half of the transmembrane segment III is shown to be involved in determining high-affinity binding of the mu-selective enkephalin-related peptides, [D-Ala2, MePhe4,Gly-ol5]enkephalin and [D-Ala2,MePhe4,Met-ol5]enkephalin, whereas the major determinant for binding of the mu-selective alkaloids, morphine and codeine, is demonstrated to exist in the region spanning the transmembrane segments V-VII. These results indicate that distinct regions of the opioid receptor determine the selectivity for the delta- and the mu-selective enkephalin-related peptides and that the binding determinant for the mu-selective alkaloids is distinct from that for the mu-selective enkephalin-related peptides.
为了阐明阿片受体分子的哪些部分参与配体选择性,我们从cDNA中表达了大鼠δ-和μ-阿片受体之间的嵌合受体,并分析了它们的配体结合特性。我们证明,δ-选择性脑啡肽相关肽[D-青霉胺2,D-青霉胺5]脑啡肽的主要结合决定簇位于包含跨膜片段V-VII和中间环区域的区域内。另一方面,从细胞内环I到跨膜片段III氨基末端一半的区域被证明参与了μ-选择性脑啡肽相关肽[D-丙氨酸2,甲硫苯丙氨酸4,甘醇5]脑啡肽和[D-丙氨酸2,甲硫苯丙氨酸4,甲硫醇5]脑啡肽高亲和力结合的决定,而μ-选择性生物碱吗啡和可待因结合的主要决定簇被证明存在于跨膜片段V-VII区域。这些结果表明,阿片受体的不同区域决定了对δ-和μ-选择性脑啡肽相关肽的选择性,并且μ-选择性生物碱的结合决定簇与μ-选择性脑啡肽相关肽的不同。