Tellez R, Allende C C, Allende J E
Departamento de Bioquímica, Facultad de Medicina, Universidad de Chile, Santiago.
FEBS Lett. 1992 Aug 17;308(2):113-5. doi: 10.1016/0014-5793(92)81255-k.
Polyglutamate analogs of folate and related compounds were tested as inhibitors of casein kinase II (CK II) obtained from Xenopus laevis. The inhibitory capacity of the pteroyl, 4-amino-10-methyl pteroyl (the methotrexate aromatic moiety), and p-aminobenzoil derivatives increased as the number of gamma-glutamates attached went from 2 to 7. The nature of the aromatic head, group was also important since hexa-gamma-glutamatic acid had no inhibitory activity while the folylhexaglutamate derivatives were strong inhibitors with relative potency of methotrexate greater than pteroyl greater than p-aminobenzoic acid. The inhibition of CK II by methotrexate gamma-pentaglutamate was competitive with casein and showed an apparent K(i) of 90 microM.
对叶酸及相关化合物的聚谷氨酸类似物作为非洲爪蟾酪蛋白激酶II(CK II)抑制剂进行了测试。蝶酰、4-氨基-10-甲基蝶酰(甲氨蝶呤的芳香部分)和对氨基苯甲酰衍生物的抑制能力随着连接的γ-谷氨酸数量从2增加到7而增强。芳香头部基团的性质也很重要,因为六γ-谷氨酸没有抑制活性,而叶酰六谷氨酸衍生物是强抑制剂,甲氨蝶呤的相对效力大于蝶酰大于对氨基苯甲酸。甲氨蝶呤γ-五谷氨酸对CK II的抑制作用与酪蛋白呈竞争性,表观抑制常数(K(i))为90微摩尔。