Harper D R, Gilbert R L, Blunt C, McIlhinney R A
Medical College, St Bartholomew's Hospital, London, U.K.
J Gen Virol. 1993 Jun;74 ( Pt 6):1181-4. doi: 10.1099/0022-1317-74-6-1181.
Inhibitors of myristoylation and analogues of myristic acid inhibit the replication of some retroviruses including human immunodeficiency virus, but no studies with other virus families have been reported. We have shown that replication of varicella-zoster virus (VZV) in tissue is inhibited by DL-2-hydroxymyristic acid at concentrations similar to those required for inhibition with acyclovir. Protein synthesis is not inhibited, but protein myristoylation is non-specifically reduced. Despite this lack of specificity, DL-2-hydroxymyristic acid inhibits VZV replication without apparent cytotoxicity. This is in agreement with our earlier suggestion that non-specific inhibitors of myristoylation could have antiviral effects without toxicity to cells due to the stability of cellular myristoylproteins. This supports suggestions that myristoylation inhibitors have potential as antiviral drugs against the many viruses that produce myristoylproteins.
肉豆蔻酰化抑制剂和肉豆蔻酸类似物可抑制包括人类免疫缺陷病毒在内的一些逆转录病毒的复制,但尚未见有关其他病毒科的研究报道。我们已经表明,DL-2-羟基肉豆蔻酸在与阿昔洛韦抑制所需浓度相似的情况下,可抑制水痘带状疱疹病毒(VZV)在组织中的复制。蛋白质合成未受抑制,但蛋白质肉豆蔻酰化被非特异性降低。尽管缺乏特异性,但DL-2-羟基肉豆蔻酸可抑制VZV复制且无明显细胞毒性。这与我们之前的观点一致,即由于细胞肉豆蔻酰蛋白的稳定性,肉豆蔻酰化的非特异性抑制剂可产生抗病毒作用而对细胞无毒。这支持了肉豆蔻酰化抑制剂有潜力作为抗多种产生肉豆蔻酰蛋白病毒的抗病毒药物的观点。