EXPRESSION CLONING OF CDNA-ENCODING A 7-HELIX RECEPTOR FROM HUMAN PLACENTA WITH AFFINITY FOR OPIOID LIGANDS

被引:41
作者
XIE, GX
MIYAJIMA, A
GOLDSTEIN, A
机构
[1] DNAX RES INST MOLEC & CELLULAR BIOL INC,PALO ALTO,CA 94304
[2] STANFORD UNIV,STANFORD,CA 94305
关键词
D O I
10.1073/pnas.89.9.4124
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Here we report the expression cloning of cDNA encoding a putative opioid receptor from a human placenta cDNA library. Placental opioid receptors are of the kappa-type. As the dynorphin opioid peptides are kappa-selective, a dynorphin ligand was used in an affinity-enrichment (panning) procedure to select transiently transfected COS-7 cells expressing kappa-receptor binding sites. The cloned cDNA encodes a 440-residue protein of the seven-helix guanine nucleotide-binding protein (G-protein)-coupled receptor family. Ligand. binding reveals a stereospecific site with typical opioid properties, which binds peptide and nonpeptide opioids with moderate affinity (K(d) almost-equal-to 100 nM) and which lacks the expected kappa-selectivity. The deduced transmembrane domain is 93% identical to the homologous region of the human neuromedin K (neurokinin B) receptor, but the N-terminal and C-terminal sequences have many dissimilarities. The expressed receptor binds opioid ligands but not tachykinins; and under the same conditions, a cloned rat neuromedin K receptor binds tachykinins but not opioids.
引用
收藏
页码:4124 / 4128
页数:5
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