Fernández S N, Mansilla-Whitacre Z C, Miceli D C
Instituto Superior de Investigaciones Biológicas, Departamento de Biología del Dessarrollo, Tucumán, Argentina.
Mol Reprod Dev. 1994 Aug;38(4):364-72. doi: 10.1002/mrd.1080380403.
Serum steroid binding properties of mature Bufo arenarum females were studied. Binding data obtained using charcoal adsorption assay and equilibrium dialysis methods indicates a single protein, named Bufo arenarum sex binding protein (Ba SBP), which binds 5 alpha-dihydrotestosterone (DHT), testosterone (T), and estradiol-17 beta (E2) with high affinity (10(-7) M-1 - 10(8) M-1) and fair capacity (10(-6) M). Scatchard plot analysis demonstrated the coexistence of two binding sites. Ba SBP has a sedimentation coefficient of 5.2 S in sucrose gradient centrifugation in low salt and under steady-state conditions. The specificity of this protein, determined by competitive binding experiments, is comparable to human SBP. DHT and T bind with higher affinity than E2. Estriol and estrone competed poorly, while diethylstilbestrol and C21 steroids did not compete. The binding capacity of this protein is under estrogenic control.
对成年雌性阿根廷蟾蜍的血清类固醇结合特性进行了研究。使用活性炭吸附测定法和平衡透析法获得的结合数据表明,存在一种单一蛋白质,名为阿根廷蟾蜍性别结合蛋白(Ba SBP),它以高亲和力(10⁻⁷ M⁻¹ - 10⁸ M⁻¹)和中等容量(10⁻⁶ M)结合5α-二氢睾酮(DHT)、睾酮(T)和雌二醇-17β(E2)。Scatchard图分析表明存在两个结合位点。在低盐和稳态条件下进行的蔗糖梯度离心实验中,Ba SBP的沉降系数为5.2 S。通过竞争性结合实验确定,该蛋白质的特异性与人类SBP相当。DHT和T的结合亲和力高于E2。雌三醇和雌酮的竞争能力较差,而己烯雌酚和C21类固醇则不参与竞争。该蛋白质的结合能力受雌激素控制。