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Bioengineers have developed a method to regulate the size and shape of virus particles by combining viral protein building blocks with DNA templates.
The resultant nanostructures may be used in vaccine development and medicine delivery inside the body. Virus capsid proteinsthe proteins that shield the genome of a viruscan be used to build precisely structured protein assemblies. Their shapes and geometry, however, depend largely on the virus strain. Reprogramming these assemblies, no matter the original viral blueprint is an intriguing possibility for drug delivery and vaccine development. Scientists tackled the challenge by generating a structured genome template on which capsid proteins can assemble. To avoid deforming the flexible genome and creating unintended shapes, they used rigidDNAorigami structures. These structures are only tens to hundreds of nanometres in length but are entirely made ofDNA, which is folded accurately into the desired template shape. "Our approach is based on electrostatic interactions between the negative charge of theDNAnanostructures and a positively charged domain of the capsid proteins, paired with intrinsic interactions between the single proteins. By altering the amount of protein used, we can fine-tune the number of highly-ordered protein layers, which encapsulate theDNAorigami," says Iris Seitz, lead author and doctoral researcher at Aalto University. "By usingDNAorigami as a template, we can direct the capsid proteins into a user-defined size and shape, resulting in assemblies that are well-defined, both in length and diameter. By testing a variety ofDNAorigami structures, we also learned how the templates geometry affected the whole assembly," Seitz adds. "With the help of cryogenic electron microscopy imaging, we were able to visualise the highly ordered proteins upon assembly and, with that, measure even small changes in the geometry of the assembly arising from different templates," explains professor Juha Huiskonen, a collaborating scientist from the University of Helsinki. "We have found a simple but effective strategy to (re)direct capsid proteins to a desired shape. Our approach is adaptable and therefore not limited to a single capsid protein type, as we demonstrated with capsid proteins from four different viruses. Additionally, we can tweak our template to be more application-relevant, for instance by integrating RNA into the origami, which could subsequently be translated into useful or site-specific proteins," explains Aalto professor Mauri Kostiainen, leader of the research project. AlthoughDNAorigami structures are a promising material for interfacing biological systems, they suffer from instability, especially in the presence ofDNA-degrading enzymes. In experiments, however, "we can clearly observe that the protein layer efficiently protects the encapsulatedDNAnanostructures from degradation. By combining protection with the functional properties of nucleic acid origami, including the possibility to deliverDNAor messenger RNA together with other cargo molecules, we believe that our approach provides interesting future directions for biomedical engineering," concludes Kostiainen. (ANI)
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