Strategies for Stabilizing DNA Nanostructures to Biological Conditions. (14th June 2019)

• Record Type: Journal Article
• Authors: Stephanopoulos, Nicholas
• Is Part Of: Chembiochem. Volume 20:Number 17(2019)
• Page Start: 2191
• Page End: 2197
• Publication Date: 2019-06-14
• Subjects: biological activity -- DNA -- nanotechnology -- polymers -- self-assembly; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pharmaceutical chemistry -- Periodicals; 572
• DOI: 10.1002/cbic.201900075
• Languages: English
• ISSNs: 1439-4227

Abstract

Abstract: DNA is one of the most promising building blocks for creating functional nanostructures for applications in biology and medicine. However, these highly programmable nanomaterials (e.g., DNA origami) often require supraphysiological salt concentrations for stability, are degraded by nuclease enzymes, and can elicit an inflammatory response. Herein, three key strategies for stabilizing DNA nanostructures to conditions required for biological applications are outlined: 1) tuning the buffer conditions or nanostructure design; 2) covalently crosslinking the strands that make up the structures; and 3) coating the structures with polymers, proteins, or lipid bilayers. Taken together, these approaches greatly expand the chemical diversity and future applicability of DNA nanotechnology both in vitro and in vivo. Abstract : Protecting the fold : Many DNA nanostructures are not stable to cell culture buffers or in vivo conditions. Tuning the buffer conditions or nanostructure design, covalently crosslinking the structures, or coating them with a protective polymer or protein layer can stabilize them and allow their application in a number of biomedical contexts.