Turning DNA Binding Motifs into a Material for Flow Cells.
Tobias FeldnerManpreet WolfrumClemens RichertPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
Nanoscale assemblies of DNA strands are readily designed and can be generated in a wide range of shapes and sizes. Turning them into solids that bind biomolecules reversibly, so that they can act as active material in flow cells, is a challenge. Among the biomolecular ligands, cofactors are of particular interest because they are often the most expensive reagents of biochemical transformations, for which controlled release and recycling are desirable. We have recently described DNA triplex motifs that bind adenine-containing cofactors, such as NAD, FAD and ATP, reversibly with low micromolar affinity. We sought ways to convert the soluble DNA motifs into a macroporous solid for cofactor binding. While assemblies of linear and branched DNA motifs produced hydrogels with undesirable properties, long DNA triplexes treated with protamine gave materials suitable for flow cells. Using exchangeable cells in a flow system, thermally controlled loading and discharge were demonstrated. Employing a flow cell loaded with ATP, bioluminescence was induced through thermal release of the cofactor. The results show that materials generated from functional DNA structures can be successfully employed in macroscopic devices.
Keyphrases
- induced apoptosis
- circulating tumor
- cell cycle arrest
- cell free
- single molecule
- dna binding
- drug delivery
- cell death
- oxidative stress
- endoplasmic reticulum stress
- signaling pathway
- pi k akt
- transcription factor
- high resolution
- mass spectrometry
- mesenchymal stem cells
- binding protein
- cancer therapy
- quantum dots
- atomic force microscopy
- high speed
- energy transfer