Tisdale M J, Phillips B J
Chem Biol Interact. 1977 Dec;19(3):375-81. doi: 10.1016/0009-2797(77)90060-6.
The intracellular level of guanosine 3',5'-monophosphate (cGMP) has been measured in Walker carcinoma cells in tissue culture after treatment with various alkylating agents. At concentrations which caused a rise in the level of adenosine 3',5'-monophosphate (cAMP) chlorambucil and 5-(1-aziridinyl)-2,4-dinitrobenzamide (CB 1954) produced only a small (35%) elevation of cGMP, while merophan had no such effect. This suggests that any effect of cAMP will not be outweighed by an equivalent rise in cGMP. Sepcific cytosolic binding of cGMP decreased with increasing resistance of Walker cells to alkylating agents, while the dissociation constant, KD, for binding increased. This was also observed with cAMP binding which suggests that the same protein in responsible for binding both nucleotides.
在用各种烷化剂处理后,对组织培养中的沃克癌细胞内的3',5'-环磷酸鸟苷(cGMP)水平进行了测定。在能引起3',5'-环磷酸腺苷(cAMP)水平升高的浓度下,苯丁酸氮芥和5-(1-氮丙啶基)-2,4-二硝基苯甲酰胺(CB 1954)仅使cGMP产生小幅(35%)升高,而美法仑则无此作用。这表明cAMP的任何作用都不会被cGMP的同等升高所抵消。随着沃克细胞对烷化剂耐药性的增加,cGMP的特异性胞质结合减少,而结合的解离常数KD增加。cAMP结合也观察到了这一点,这表明负责结合这两种核苷酸的是同一种蛋白质。