Ishihara H, Martin B L, Brautigan D L, Karaki H, Ozaki H, Kato Y, Fusetani N, Watabe S, Hashimoto K, Uemura D
Muscle Biol. Group, Univ. of Arizona, Tucson 85721.
Biochem Biophys Res Commun. 1989 Mar 31;159(3):871-7. doi: 10.1016/0006-291x(89)92189-x.
Calyculin A and okadaic acid induce contraction in smooth muscle fibers. Okadaic acid is an inhibitor of phosphatase activity and the aims of this study were to determine if calyculin A also inhibits phosphatase and to screen effects of both compounds on various phosphatases. Neither compound inhibited acid or alkaline phosphatases, nor the phosphotyrosine protein phosphatase. Both compounds were potent inhibitors of the catalytic subunit of type-2A phosphatase, with IC50 values of 0.5 to 1 nM. With the catalytic subunit of protein phosphatase type-1, calyculin A was a more effective inhibitor than okadaic acid, IC50 values for calyculin A were about 2 nM and for okadaic acid between 60 and 500 nM. The endogenous phosphatase of smooth muscle myosin B was inhibited by both compounds with IC50 values of 0.3 to 0.7 nM and 15 to 70 nM, for calyculin A and okadaic acid, respectively. The partially purified catalytic subunit from myosin B had IC50 values of 0.7 and 200 nM for calyculin A and okadaic acid, respectively. The pattern of inhibition for the phosphatase in myosin B therefore is similar to that of the type-1 enzyme.
花萼海绵诱癌素A和冈田酸可诱导平滑肌纤维收缩。冈田酸是一种磷酸酶活性抑制剂,本研究的目的是确定花萼海绵诱癌素A是否也抑制磷酸酶,并筛选这两种化合物对各种磷酸酶的作用。这两种化合物均未抑制酸性或碱性磷酸酶,也未抑制磷酸酪氨酸蛋白磷酸酶。这两种化合物都是2A型磷酸酶催化亚基的有效抑制剂,IC50值为0.5至1 nM。对于1型蛋白磷酸酶的催化亚基,花萼海绵诱癌素A是比冈田酸更有效的抑制剂,花萼海绵诱癌素A的IC50值约为2 nM,冈田酸的IC50值在60至500 nM之间。平滑肌肌球蛋白B的内源性磷酸酶被这两种化合物抑制,花萼海绵诱癌素A和冈田酸的IC50值分别为0.3至0.7 nM和15至70 nM。从肌球蛋白B中部分纯化的催化亚基对花萼海绵诱癌素A和冈田酸的IC50值分别为0.7和200 nM。因此,肌球蛋白B中磷酸酶的抑制模式与1型酶相似。