Ohtsuki K, Iahida N
Department of Bioscience, Kitasato University School of Hygienic Sciences, Kanagawa, Japan.
Biochem Biophys Res Commun. 1988 Dec 15;157(2):597-604. doi: 10.1016/s0006-291x(88)80292-4.
The anti-viral mechanism of glycyrrhizin (GL) has been investigated by considering in vitro effects on polypeptide phosphorylation. It was found that GL (i), at low doses, selectively inhibits protein phosphorylation by Kinase P, but has not significant effects on the activities of other kinases (Kinase A, Kinase C and histone kinase); (ii) binds directly to Kinase P and reduces kinase activity in a dose-dependent manner; and (iii) inhibits vesicular stomatitis virus (VSV)-associated kinase activity. These observations strongly suggest that direct binding of GL to the virus causes the direct inactivation of virus-associated kinase and the reduction of the viral infectivity.
通过考虑甘草酸(GL)对多肽磷酸化的体外作用,研究了其抗病毒机制。结果发现,GL(i)在低剂量时可选择性抑制激酶P介导的蛋白质磷酸化,但对其他激酶(激酶A、激酶C和组蛋白激酶)的活性无显著影响;(ii)直接与激酶P结合,并以剂量依赖的方式降低激酶活性;(iii)抑制水疱性口炎病毒(VSV)相关激酶活性。这些观察结果强烈表明,GL与病毒的直接结合导致病毒相关激酶直接失活并降低病毒感染力。