Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 171 77 Stockholm, Sweden.
Viruses. 2018 Feb 28;10(3):105. doi: 10.3390/v10030105.
Alphaviruses encode 4 non-structural proteins (nsPs), most of which have well-understood functions in capping and membrane association (nsP1), polyprotein processing and RNA helicase activity (nsP2) and as RNA-dependent RNA polymerase (nsP4). The function of nsP3 has been more difficult to pin down and it has long been referred to as the more enigmatic of the nsPs. The protein comprises three domains, an N-terminal macro domain, a central zinc-binding domain and a C-terminal hypervariable domain (HVD). In this article, we review old and new literature about the functions of the three domains. Much progress in recent years has contributed to a picture of nsP3, particularly through its HVD as a hub for interactions with host cell molecules, with multiple effects on the biology of the host cell at early points in infection. These and many future discoveries will provide targets for anti-viral therapies as well as strategies for modification of vectors for vaccine and oncolytic interventions.
甲病毒编码 4 种非结构蛋白(nsPs),其中大多数在加帽和膜结合(nsP1)、多蛋白加工和 RNA 解旋酶活性(nsP2)以及 RNA 依赖性 RNA 聚合酶(nsP4)方面具有明确的功能。nsP3 的功能更难确定,长期以来一直被称为 nsPs 中更神秘的蛋白。该蛋白包含三个结构域,一个 N 端的宏结构域、一个中央锌结合结构域和一个 C 端的超变结构域(HVD)。在本文中,我们回顾了有关这三个结构域功能的旧文献和新文献。近年来的许多进展有助于我们了解 nsP3 的功能,特别是通过其 HVD 作为与宿主细胞分子相互作用的中心,在感染早期对宿主细胞的生物学产生多种影响。这些以及许多未来的发现将为抗病毒疗法提供靶点,并为疫苗和溶瘤干预载体的修饰提供策略。