Programmable icosahedral shell system for virus trapping

Broad spectrum antiviral platforms that can decrease or inhibit viral infection would alleviate many threats to global public health. Nonetheless, effective technologies of this kind are still not available. Here we describe a programmable icosahedral canvas for the self-assembly of icosahedral shells that have viral trapping and antiviral properties. Programmable triangular building blocks constructed from DNA assemble with high yield into various shell objects with user-defined geometries and apertures. We create shells with molecular masses ranging from 43 to 925 Megadaltons (8 to 180 subunits) and with internal cavity diameters ranging up to 280 nm. The shell interior can be functionalized with virus-specific moieties in a modular fashion. We demonstrate this virus-trap concept by engulfing hepatitis B virus (HBV) core particles and adeno-associated viruses (AAV). We show inhibition of HBV core interactions with surfaces in vitro and demonstrate neutralization of infectious AAV exposed to human cells.