Uncoating Mechanism of Carnation Mottle Virus Revealed by Cryo-EM Single Particle Analysis

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Chun-Yan Wang
Qin-Fen Zhang
Yuan-Zhu Gao
Li Xie
Hong-Mei Li
Jian Hong
Chuan-Xi Zhang
机构
[1] College of Agriculture and Biotechnology,
[2] Zhejiang University,undefined
[3] State Key Laboratory of Biocontrol,undefined
[4] School of Life Sciences,undefined
[5] Sun Yat-sen University,undefined
[6] Institute of Virology and Biotechnology,undefined
[7] Zhejiang Academy of Agricultural Sciences,undefined
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Genome uncoating is a prerequisite for the successful infection of plant viruses in host plants. Thus far, little is known about the genome uncoating of the Carnation mottle virus (CarMV). Here, we obtained two reconstructions of CarMV at pH7 in the presence (Ca-pH7) and absence (EDTA-pH7) of calcium ions by Cryo-EM single particle analysis, which achieved 6.4 Å and 8 Å resolutions respectively. Our results showed that chelation of the calcium ions under EDTA-pH7 resulted in reduced interaction between the subunits near the center of the asymmetric unit but not overall size change of the viral particles, which indicated that the role of the calcium ions in CarMV was not predominantly for the structural preservation. Part of the genomic RNA closest to the capsid was found to be located near the center of the asymmetric unit, which might result from the interaction between genomic RNA and Lys194 residues. Together with the electrostatic potential analysis on the inner surface of the asymmetric unit, the reduced interaction near the center of the asymmetric unit under EDTA-pH7 suggested that the genome release of CarMV might be realized through the center of the asymmetric unit.
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