Sarmiento J G, Epstein P M, Rowe W A, Chester D W, Smilowitz H, Wehinger E, Janis R A
Life Sci. 1986 Dec 22;39(25):2401-9. doi: 10.1016/0024-3205(86)90481-9.
The binding sites for Ca2+ channel antagonists were probed using Bay P 8857 [2-iodoethyl isopropyl 1,4-dihydropyridine-2,6-dimethyl-4-(3-nitrophenyl)-pyridine-3,5-dicarbox ylate] that has been radiolabelled with 125I. This drug was shown to bind with high affinity to cardiac, smooth, and skeletal muscle membranes, with a KD approximately equal to 0.3 nM. A protein of molecular weight 33-35,000 daltons was specifically and irreversibly radiolabelled after irradiation of cardiac, skeletal and aortic smooth muscle membranes, incubated with the [125I]-Bay P 8857. The peptide labelled by 1,4-dihydropyridine binding therefore appears similar in size for cardiac, skeletal, and smooth muscle. This data suggests that of the three peptide subunits which reportedly comprise the skeletal and cardiac muscle 1,4-dihydropyridine receptor complex, the 33-35,000 dalton peptide contains the dihydropyridine binding site.
使用已用¹²⁵I放射性标记的Bay P 8857 [2-碘乙基异丙基1,4-二氢吡啶-2,6-二甲基-4-(3-硝基苯基)-吡啶-3,5-二羧酸酯]来探测Ca²⁺通道拮抗剂的结合位点。已证明该药物能以高亲和力与心脏、平滑肌和骨骼肌膜结合,解离常数(KD)约等于0.3 nM。在与[¹²⁵I]-Bay P 8857一起孵育的心脏、骨骼肌和主动脉平滑肌膜经照射后,一种分子量为33000 - 35000道尔顿的蛋白质被特异性且不可逆地放射性标记。因此,由1,4-二氢吡啶结合所标记的肽在心脏、骨骼肌和平滑肌中的大小似乎相似。该数据表明,在据报道构成骨骼肌和心肌1,4-二氢吡啶受体复合物的三个肽亚基中,33000 - 35000道尔顿的肽含有二氢吡啶结合位点。