Description
EMD-16076: Helical shell of CCMV capsid protein on DNA origami 6HB-2k
Sample Organism: Cowpea chlorotic mottle virus
Sample: Helical shell of CCMV capsid protein on DNA origami 6HB-2k
Primary publication: DNA-origami-directed virus capsid polymorphism.
Viral capsids can adopt various geometries, most iconically characterized by icosahedral or helical symmetries. Importantly, precise control over the size and shape of virus capsids would have advantages in the development of new vaccines and delivery systems. However, current tools to direct the assembly process in a programmable manner are exceedingly elusive. Here we introduce a modular approach by demonstrating DNA-origami-directed polymorphism of single-protein subunit capsids. We achieve control over the capsid shape, size and topology by employing user-defined DNA origami nanostructures as binding and assembly platforms, which are efficiently encapsulated within the capsid. Furthermore, the obtained viral capsid coatings can shield the encapsulated DNA origami from degradation. Our approach is, moreover, not limited to a single type of capsomers and can also be applied to RNA-DNA origami structures to pave way for next-generation cargo protection and targeting strategies.
Sample Organism: Cowpea chlorotic mottle virus
Sample: Helical shell of CCMV capsid protein on DNA origami 6HB-2k
Primary publication: DNA-origami-directed virus capsid polymorphism.
Viral capsids can adopt various geometries, most iconically characterized by icosahedral or helical symmetries. Importantly, precise control over the size and shape of virus capsids would have advantages in the development of new vaccines and delivery systems. However, current tools to direct the assembly process in a programmable manner are exceedingly elusive. Here we introduce a modular approach by demonstrating DNA-origami-directed polymorphism of single-protein subunit capsids. We achieve control over the capsid shape, size and topology by employing user-defined DNA origami nanostructures as binding and assembly platforms, which are efficiently encapsulated within the capsid. Furthermore, the obtained viral capsid coatings can shield the encapsulated DNA origami from degradation. Our approach is, moreover, not limited to a single type of capsomers and can also be applied to RNA-DNA origami structures to pave way for next-generation cargo protection and targeting strategies.
| Date made available | 5 Jul 2023 |
|---|---|
| Publisher | Protein Data Bank (PDB) |
Funding
| Funders |
|---|
| OtaNanoNanomicroscopy Center |
| Horizon 2020 Framework Programme |
| European Research Council |
| Academy of Finland |
| Aalto-yliopisto |
| Jane ja Aatos Erkon Säätiö |
| China Scholarship Council |
| Emil Aaltosen Säätiö |
| Tekniikan Edistämissäätiö |
| Sigrid Juséliuksen Säätiö |
| Biocenter Finland |
Field of science, Statistics Finland
- 1182 Biochemistry, cell and molecular biology
- 1183 Plant biology, microbiology, virology
Research output
- 1 Article
-
DNA-origami-directed virus capsid polymorphism
Seitz, I., Saarinen, S., Kumpula, E.-P., McNeale, D., Anaya-Plaza, E., Lampinen, V., Hytönen, V. P., Sainsbury, F., Cornelissen, J. J. L. M., Linko, V., Huiskonen, J. T. & Kostiainen, M. A., 2023, In: Nature Nanotechnology. 18, p. 1205-1212 11 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile40 Citations (Scopus)32 Downloads (Pure)
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