TY - JOUR
T1 - DNA-origami-directed virus capsid polymorphism
AU - Seitz, Iris
AU - Saarinen, Sharon
AU - Kumpula, Esa Pekka
AU - McNeale, Donna
AU - Anaya-Plaza, Eduardo
AU - Lampinen, Vili
AU - Hytönen, Vesa P.
AU - Sainsbury, Frank
AU - Cornelissen, Jeroen J.L.M.
AU - Linko, Veikko
AU - Huiskonen, Juha T.
AU - Kostiainen, Mauri A.
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/10
Y1 - 2023/10
N2 - 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.
AB - 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.
KW - Nanobiotechnology
KW - Nanoparticles
KW - Nanostructures
UR - http://www.scopus.com/inward/record.url?scp=85164964063&partnerID=8YFLogxK
U2 - 10.1038/s41565-023-01443-x
DO - 10.1038/s41565-023-01443-x
M3 - Article
C2 - 37460794
AN - SCOPUS:85164964063
SN - 1748-3387
VL - 18
SP - 1205
EP - 1212
JO - Nature nanotechnology
JF - Nature nanotechnology
IS - 10
ER -