Mihara H, Lee S, Shimohigashi Y, Aoyagi H, Kato T, Izumiya N, Costa T
FEBS Lett. 1985 Nov 25;193(1):35-8. doi: 10.1016/0014-5793(85)80074-0.
The fluorescent amino acid, L-1-pyrenylalanine (Pya) was incorporated into [D-Ala2,Leu5]enkephalin and its methyl ester at position 4 or 5. Pya-enkephalins showed strong fluorescent intensity and displayed high binding affinity for opiate receptors. Pya4-enkephalins showed high specificity for the mu receptors, while Pya5-enkephalins showed high specificity and selectivity for the delta receptors. Particularly, [D-Ala2,Pya5]enkephalin was as potent as the most utilized delta-specific ligand of [D-Ala2,D-Leu5]enkephalin (DADLE), and yet its delta-selectivity was about 5-times greater than that of DADLE. Thus, Pya-enkephalins per se can be utilized as a fluorescent probe or tracer for the opiate receptor-binding assays.
将荧光氨基酸L-1-芘丙氨酸(Pya)掺入[D-丙氨酸2,亮氨酸5]脑啡肽及其甲酯的第4或第5位。Pya-脑啡肽显示出很强的荧光强度,并对阿片受体表现出高结合亲和力。Pya4-脑啡肽对μ受体具有高特异性,而Pya5-脑啡肽对δ受体具有高特异性和选择性。特别地,[D-丙氨酸2,Pya5]脑啡肽与最常用的δ特异性配体[D-丙氨酸2,D-亮氨酸5]脑啡肽(DADLE)一样有效,但其δ选择性比DADLE大约5倍。因此,Pya-脑啡肽本身可用作阿片受体结合测定的荧光探针或示踪剂。