摘要
与人类慢性疾病有关的核糖核酸(RNA)病毒是对公共健康的主要威胁,在全球范围内造成很高的死亡率。 RNA病毒的高突变率有助于它们逃避免疫反应,并且还引起耐药性的发展。人类免疫缺陷病毒(HIV)和肝炎病毒(HBV和HCV)引起的慢性感染分别导致获得性免疫缺陷综合症(AIDS)和肝细胞癌,这是人类死亡的主要原因之一。绝对有必要采取有效的预防措施,以限制慢性和再次出现的病毒感染。每类抗病毒剂都针对病毒生命周期中的特定阶段,并抑制其发展和增殖。大多数情况下,抗病毒药物靶向特定的病毒蛋白,因此只有少数几种广谱药物可用。这篇综述将集中在病原性病毒的选定病毒靶蛋白上,这些病原性病毒包含导致人类慢性感染的单链(ss)RNA基因组(例如HIV,HCV,黄病毒)。在最近的过去,可用的三维蛋白质结构数量呈指数级增长(在蛋白质数据库中> 150000),使我们能够更好地了解蛋白质靶标和抗病毒药物的分子机制。电子计算机方法的进步为设计和开发针对病毒蛋白的新型,高特异性小分子抑制剂铺平了道路。
关键词: RNA病毒,慢性疾病,药物靶标,抑制剂,抗病毒剂,HIV,肝炎,黄病毒,蛋白质结构。
图形摘要
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