Yokoyama N, Murota Y, Negishi T, Saito M, Furuyama S
Can J Physiol Pharmacol. 1983 Feb;61(2):109-14. doi: 10.1139/y83-015.
Cyclic GMP phosphodiesterase was investigated in the submandibular gland of the adult rat to elucidate the regulatory mechanisms of cGMP concentration in this gland. Ca2+ sensitivity was easily demonstrated as in other tissues using EGTA in the buffer for elution from DEAE-cellulose. The presence of inhibitor proteins for basal and calmodulin-activated portions of Ca2+-dependent phosphodiesterase was suggested. The inhibitor for the basal activity of Ca2+-dependent phosphodiesterase was deemed to be a heat-labile protein, which decreased Vmax, but had no effect on the Km value for cGMP. The presence of more than one kind of inhibitor for the calmodulin-activated portion of the Ca2+-dependent phosphodiesterase was also suggested. One of these, which was not absorbed on DEAE-cellulose, was a heat-labile protein which caused an increase of Km for cGMP, but no change of Vmax.
为阐明成年大鼠下颌下腺中cGMP浓度的调节机制,对环鸟苷酸磷酸二酯酶进行了研究。使用EGTA作为从DEAE-纤维素洗脱的缓冲液中的成分,Ca2+敏感性与其他组织一样很容易得到证明。研究表明存在针对钙依赖性磷酸二酯酶基础活性部分和钙调蛋白激活部分的抑制蛋白。钙依赖性磷酸二酯酶基础活性的抑制剂被认为是一种热不稳定蛋白,它降低了Vmax,但对cGMP的Km值没有影响。研究还表明存在不止一种针对钙依赖性磷酸二酯酶钙调蛋白激活部分的抑制剂。其中一种不被DEAE-纤维素吸附的抑制剂是一种热不稳定蛋白,它导致cGMP的Km增加,但Vmax没有变化。