Nakano Masahiro, Noda Takeshi
Laboratory of Ultrastructural Virology, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Graduate School of Biostudies, Kyoto University, Kyoto, Japan.
Methods Mol Biol. 2025;2890:141-149. doi: 10.1007/978-1-0716-4326-6_7.
Influenza A virus (IAV) has an eight-segmented, single-stranded, negative-sense viral genomic RNA (vRNA). Each vRNA strand associates with nucleoproteins and an RNA-dependent RNA polymerase complex to form a viral ribonucleoprotein (vRNP) complex. IAV vRNPs adopt a flexible double-helical configuration that varies in length. Although the transcription and replication of vRNA take place in the context of vRNPs, the precise structural conformation of vRNPs during RNA synthesis remains partially elucidated. To unravel the intricate ultrastructure of the vRNP, it is necessary to purify it while preserving its native functionality. Herein, we introduce a comprehensive protocol for the purification of IAV vRNPs using glycerol gradient ultracentrifugation. Furthermore, we provide a method for the high-speed atomic force microscopy observation of vRNPs during viral RNA synthesis.
甲型流感病毒(IAV)具有八段单链负义病毒基因组RNA(vRNA)。每条vRNA链与核蛋白及RNA依赖性RNA聚合酶复合物结合,形成病毒核糖核蛋白(vRNP)复合物。IAV vRNP采用长度可变的灵活双螺旋结构。尽管vRNA的转录和复制在vRNP的背景下发生,但RNA合成过程中vRNP的确切结构构象仍部分有待阐明。为了解开vRNP复杂的超微结构,有必要在保留其天然功能的同时对其进行纯化。在此,我们介绍一种使用甘油梯度超速离心法纯化IAV vRNP的综合方案。此外,我们还提供一种在病毒RNA合成过程中对vRNP进行高速原子力显微镜观察的方法。