4.5 Article

RNA nanotechnology to build a dodecahedral genome of single-stranded RNA virus

期刊

RNA BIOLOGY
卷 18, 期 12, 页码 2390-2400

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/15476286.2021.1915620

关键词

RNA nanotechnology; RNA nanostructures; cage; dodecahedral viral genome

资金

  1. NIH [U01CA151648, R01EB019036, P41GM103832, S10 OD021600, R01 GM096039, R01 GM118006]
  2. CM Chen Foundation

向作者/读者索取更多资源

The quest for artificial RNA viral complexes with authentic structure while being non-replicative is advancing for the development of viral vaccines. Progress in virus-inspired nanotechnology has been fueled by the unique structural and functional properties of viruses.
The quest for artificial RNA viral complexes with authentic structure while being non-replicative is on its way for the development of viral vaccines. RNA viruses contain capsid proteins that interact with the genome during morphogenesis. The sequence and properties of the protein and genome determine the structure of the virus. For example, the Pariacoto virus ssRNA genome assembles into a dodecahedron. Virus-inspired nanotechnology has progressed remarkably due to the unique structural and functional properties of viruses, which can inspire the design of novel nanomaterials. RNA is a programmable biopolymer able to self-assemble sophisticated 3D structures with rich functionalities. RNA dodecahedrons mimicking the Pariacoto virus quasi-icosahedral genome structures were constructed from both native and 2MODIFIER LETTER PRIME-F modified RNA oligos. The RNA dodecahedron easily self-assembled using the stable pRNA three-way junction of bacteriophage phi29 as building blocks. The RNA dodecahedron cage was further characterized by cryo-electron microscopy and atomic force microscopy, confirming the spontaneous and homogenous formation of the RNA cage. The reported RNA dodecahedron cage will likely provide further studies on the mechanisms of interaction of the capsid protein with the viral genome while providing a template for further construction of the viral RNA scaffold to add capsid proteins for the assembly of the viral nucleocapsid as a model. Understanding the self-assembly and RNA folding of this RNA cage may offer new insights into the 3D organization of viral RNA genomes. The reported RNA cage also has the potential to be explored as a novel virus-inspired nanocarrier.

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