
The unique ability of complementary DNA sequences to recognize and assemble as duplexes is the biochemical mechanism for how genes are read and copied. The rules of duplex formation (also called hybridization) are simple and invariable, making them predictable and programmable too. Programming DNA hybridization allows for synthetic genes to be assembled and large-scale nanostructures to be built. This process always relies on perfect sequence complementarity. Programming instability vastly expands our ability to manipulate molecular structure and has applications in the field of DNA and RNA therapeutics. In this novel study, researchers at the Institute of Inorganic Chemistry at the University of Vienna showed that controlled hybridization can result in the creation of 16 million colors and can accurately reproduce any digital To do so, the research team used a method for parallel DNA synthesis called maskless array synthesis (MAS). With MAS, hundreds of thousands of unique DNA sequences can be synthesized at the same time and on the same surface, a miniature rectangle the size of a fingernail. Since the approach allows the experimenter to control the location of any DNA sequence on that surface, the corresponding color can also be selectively assigned to a chosen location. By automating the process using dedicated computer scripts, the authors were able to transform any digital image into a DNA photocopy with accurate color rendition. "Essentially, our synthesis surface becomes a canvas for painting with DNA molecules at the micrometer scale", says Jory Lietard, PI in the Institute of Inorganic Chemistry.

This work was financially supported by the Austrian Science Fund (FWF projects I4923, P34284, P36203 and TAI687).
Original publication:

T. Kekic, J. Lietard: A Canvas of Spatially Arranged DNA Strands that Can Produce 24-bit Color Depth. Journal of the American Chemical Society. Published online October 4, 2023.
DOI: 10.1021/jacs.3c06500