Azhaeva E V, Severin E S
Bioorg Khim. 1987 Sep;13(9):1157-63.
cGMP-dependent cyclic nucleotide phosphodiesterases have been isolated from spleen lymphocytes and the whole mice spleen and shown to possess identical properties. Two structure analogues of cAMP and cGMP, viz. N6,O2'-dibutyryl-cAMP and N2,O2'-dibutyryl-cGMP, were used to investigate the properties of the phosphodiesterase and found to inhibit hydrolysis of both cAMP and cGMP. This inhibition did not affect the cGMP activation constant. Existence of two different centres of catalytic and regulatory types in cGMP-stimulated phosphodiesterase is suggested.
已从脾淋巴细胞和全小鼠脾脏中分离出依赖于环磷酸鸟苷(cGMP)的环核苷酸磷酸二酯酶,并证明其具有相同的特性。使用两种环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)的结构类似物,即N6,O2'-二丁酰-cAMP和N2,O2'-二丁酰-cGMP,来研究磷酸二酯酶的特性,发现它们可抑制cAMP和cGMP的水解。这种抑制作用不影响cGMP的激活常数。提示在cGMP刺激的磷酸二酯酶中存在两种不同类型的催化和调节中心。