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8BI4

Helical shell of CCMV capsid protein on DNA origami 6HB-2k

Summary for 8BI4
Entry DOI10.2210/pdb8bi4/pdb
EMDB information16076
DescriptorCoat protein (1 entity in total)
Functional Keywordsorigami, capsid, virus like particle
Biological sourceCowpea chlorotic mottle virus
Total number of polymer chains6
Total formula weight122017.51
Authors
Kumpula, E.-P.,Seitz, I.,Kostiainen, M.A.,Huiskonen, J.T. (deposition date: 2022-11-01, release date: 2023-07-05, Last modification date: 2023-10-25)
Primary citationSeitz, I.,Saarinen, S.,Kumpula, E.P.,McNeale, D.,Anaya-Plaza, E.,Lampinen, V.,Hytonen, V.P.,Sainsbury, F.,Cornelissen, J.J.L.M.,Linko, V.,Huiskonen, J.T.,Kostiainen, M.A.
DNA-origami-directed virus capsid polymorphism.
Nat Nanotechnol, 18:1205-1212, 2023
Cited by
PubMed Abstract: 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.
PubMed: 37460794
DOI: 10.1038/s41565-023-01443-x
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.3 Å)
Structure validation

227111

数据于2024-11-06公开中

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