Yura Y, Kusaka J, Kondo Y, Tsujimoto H, Yoshida H, Sato M
Second Department of Oral and Maxillofacial Surgery, Tokushima University School of Dentistry, Japan.
Arch Virol. 1995;140(7):1181-94. doi: 10.1007/BF01322745.
Tyrphostins 9 and 47, inhibitors of protein-tyrosine kinase, inhibited the replication of herpes simplex virus type 1 (HSV-1), whereas tyrophostin 1, which does not inhibit protein-tyrosine kinase, did not affect the replication of HSV-1. The inhibitory effect of tyrphostin 9 was more potent than that of tyrphostin 47, and the IC50 of tyrphostin 9 was 40 nM. Sodium orthovanadate, an inhibitor of protein phosphotyrosine phosphatase, increased HSV-1 plaque formation and its effect was partly reversed by tyrphostin 9. The phosphorylation of viral phosphoproteins was decreased by tyrphostin 9 in a dose-dependent manner, but the tyrphostin 9-induced reduction of protein synthesis was not dose-dependent. At the late stage of infection, tyrosine phosphorylation was demonstrated in HSV-1 phosphoproteins. These results indicate that protein-tyrosine kinase is involved in the replication of HSV-1 and that tyrphostin can inhibit the synthesis and post-translational phosphorylation of the viral proteins.
蛋白酪氨酸激酶抑制剂 tyrphostins 9 和 47 可抑制单纯疱疹病毒 1 型(HSV - 1)的复制,而不抑制蛋白酪氨酸激酶的 tyrphostin 1 对 HSV - 1 的复制没有影响。tyrphostin 9 的抑制作用比 tyrphostin 47 更强,tyrphostin 9 的 IC50 为 40 nM。蛋白磷酸酪氨酸磷酸酶抑制剂原钒酸钠可增加 HSV - 1 蚀斑形成,其作用部分被 tyrphostin 9 逆转。tyrphostin 9 可使病毒磷蛋白的磷酸化呈剂量依赖性降低,但 tyrphostin 9 诱导的蛋白质合成减少不呈剂量依赖性。在感染后期,HSV - 1 磷蛋白中出现酪氨酸磷酸化。这些结果表明蛋白酪氨酸激酶参与了 HSV - 1 的复制,且 tyrphostin 可抑制病毒蛋白的合成及翻译后磷酸化。