Using the components of a particularly Well-Studied plant virus, cowpea chlorotic mottle virus (CCMV), we demonstrate the synthesis of virus like particles (VLPs) with one end of the packaged RNA extending out of the capsid and into the surrounding Solution: This construct breaks the otherwise perfect symmetry of the capsid and provides a straightforward route for monofunctionalizing VLPS using the principles Of DNA nanotechnology. It also allows physical manipulation of the packaged RNA, a previously inaccessible part of the viral architecture. Our synthesis does not involve covalent chemistry Of any kind; rather, We trigger capsid assembly oh a scaffold of Viral:RNA that is hybridized atone end to a complementary DNA strand Interaction of CCMV capsid protein with this RNA DNA template leads to,selective packaging of the RNA portion into a: well formed capsid but leaves the hybridized: portion poking out the capsid through a small hole. We show that the nucleic acid protruding from the capsid is capable of :binding free DNA strands: and DNA-functionalized colloidal particles. Separately, we show that the RNA-DNA scaffold tan he used to nucleate virus formation on a DNA-functionalized surface. We believe this self-assembly strategy can be adapted to viruses other than CCMV..