Department of Biosciences.
J Virol. 2013 Dec;87(24):13279-86. doi: 10.1128/JVI.02285-13. Epub 2013 Oct 2.
Many complex viruses use an assembly pathway in which their genome is packaged into an empty procapsid which subsequently matures into its final expanded form. We utilized Pseudomonas phage 6, a well-established virus assembly model, to probe the plasticity of the procapsid maturation pathway. The 6 packaging nucleoside triphosphatase (NTPase), which powers sequential translocation of the three viral genomic single-stranded RNA molecules to the procapsid during capsid maturation, is part of the mature 6 virion but may spontaneously be dissociated from the procapsid shell. We demonstrate that the dissociation of NTPase subunits results in premature capsid expansion, which is detected as a change in the sedimentation velocity and as defects in RNA packaging and transcription activity. However, this dead-end conformation of the procapsids was rescued by the addition of purified NTPase hexamers, which efficiently associated on the NTPase-deficient particles and subsequently drove their contraction to the compact naive conformation. The resulting particles regained their biological and enzymatic activities, directing them into a productive maturation pathway. These observations imply that the maturation pathways of complex viruses may contain reversible steps that allow the rescue of the off-pathway conformation in an overall unidirectional virion assembly pathway. Furthermore, we provide direct experimental evidence that particles which have different physical properties (distinct sedimentation velocities and conformations) display different stages of the genome packaging program and show that the transcriptional activity of the 6 procapsids correlates with the number of associated NTPase subunits.
许多复杂的病毒使用一种组装途径,将其基因组包装到空的原衣壳中,然后原衣壳进一步成熟为最终的扩展形式。我们利用假单胞菌噬菌体 6 作为一种成熟的病毒组装模型,来探测原衣壳成熟途径的可塑性。6 包装核苷三磷酸酶 (NTPase) 在衣壳成熟过程中推动三个病毒基因组单链 RNA 分子连续转移到原衣壳中,是成熟的 6 病毒粒子的一部分,但可能会自发地从原衣壳壳中解离。我们证明,NTPase 亚基的解离会导致衣壳过早扩张,这表现为沉降速度的变化以及 RNA 包装和转录活性的缺陷。然而,通过添加纯化的 NTPase 六聚体可以挽救原衣壳的这种无出路的构象,NTPase 六聚体有效地与 NTPase 缺陷颗粒结合,并随后驱动它们收缩到紧凑的原始构象。得到的颗粒恢复了它们的生物学和酶学活性,引导它们进入一个有生产力的成熟途径。这些观察结果表明,复杂病毒的成熟途径可能包含可逆步骤,允许在整体单向病毒衣壳组装途径中挽救偏离途径的构象。此外,我们提供了直接的实验证据,表明具有不同物理性质(不同的沉降速度和构象)的颗粒显示出基因组包装程序的不同阶段,并且表明 6 原衣壳的转录活性与结合的 NTPase 亚基数量相关。