Sourimant Julien, Plemper Richard K
Institute for Biomedical Sciences, Georgia State University, 100 Piedmont Av, Atlanta, GA 30303, USA.
Viruses. 2016 Sep 10;8(9):251. doi: 10.3390/v8090251.
The morbillivirus genus comprises major human and animal pathogens, including the highly contagious measles virus. Morbilliviruses feature single stranded negative sense RNA genomes that are wrapped by a plasma membrane-derived lipid envelope. Genomes are encapsidated by the viral nucleocapsid protein forming ribonucleoprotein complexes, and only the encapsidated RNA is transcribed and replicated by the viral RNA-dependent RNA polymerase (RdRp). In this review, we discuss recent breakthroughs towards the structural and functional understanding of the morbillivirus polymerase complex. Considering the clinical burden imposed by members of the morbillivirus genus, the development of novel antiviral therapeutics is urgently needed. The viral polymerase complex presents unique structural and enzymatic properties that can serve as attractive candidates for druggable targets. We evaluate distinct strategies for therapeutic intervention and examine how high-resolution insight into the organization of the polymerase complex may pave the path towards the structure-based design and optimization of next-generation RdRp inhibitors.
麻疹病毒属包含主要的人类和动物病原体,包括具有高度传染性的麻疹病毒。麻疹病毒的特征是单链负义RNA基因组,其被源自质膜的脂质包膜包裹。基因组由病毒核衣壳蛋白衣壳化,形成核糖核蛋白复合物,并且只有衣壳化的RNA由病毒RNA依赖性RNA聚合酶(RdRp)转录和复制。在本综述中,我们讨论了在对麻疹病毒聚合酶复合物的结构和功能理解方面的最新突破。考虑到麻疹病毒属成员所带来的临床负担,迫切需要开发新型抗病毒疗法。病毒聚合酶复合物具有独特的结构和酶学特性,可作为有吸引力的可成药靶点候选物。我们评估了不同的治疗干预策略,并研究了对聚合酶复合物组织的高分辨率洞察如何为基于结构的下一代RdRp抑制剂的设计和优化铺平道路。