A facile and reproducible method for the purification of peptide- and protein-functionalized DNA nanostructures
Izar SchärfiD, Anna Paton, Betül Karakoc, Bianca Greul, Anna ScheederiD, Paraskevi NaniiD, Pilar PerisiD, Maria ZacharopoulouiD, Viktorija GlembockyteiD, Ioanna MelaiD
Abstract
DNA nanotechnology has emerged as a promising field for biomedical applications, both in the therapeutic and diagnostic domains. The ability of DNA nanostructures to carry cargos in precise numbers and orientations, makes them competitive candidates for drug delivery, biosensors or imaging agents. Two of the main challenges for translating DNA nanostructures from the laboratory to the clinic are achieving cost-effective largescale production and establishing comprehensive safety profiles. Having the ability to reliably and efficiently purify functionalized DNA nanostructures is key to both challenges, and an open question in the field of DNA nanotechnology. Here, we present a scalable method for the fast and efficient purification of high concentration of peptide- or protein-functionalized DNA nanostructures. We use a gravity-driven size exclusion chromatography approach, that has the potential to purify DNA nanostructures within 10 minutes, with yield up to 93% and purity up to 99% and is appropriate for both protein and peptide conjugates. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=71 SRC="FIGDIR/small/658483v1_ufig1.gif" ALT="Figure 1"> View larger version (19K): org.highwire.dtl.DTLVardef@4e3ea5org.highwire.dtl.DTLVardef@f2f615org.highwire.dtl.DTLVardef@fa042aorg.highwire.dtl.DTLVardef@27942a_HPS_FORMAT_FIGEXP M_FIG C_FIG
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