Photo-induced chemistry for the design of oligonucleotide conjugates and surfaces

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Abstract

A photocaged diene is introduced at the 5′-end of oligonucleotides using the H-phosphonate approach. The photoenol-functionalized DNA is subsequently employed for the conjugation to a protein and the spatially controlled immobilization onto surfaces using a light-induced Diels-Alder cycloaddition. Fully functional protein-DNA conjugates and patterned DNA surfaces are obtained under mild irradiation conditions.

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Vigovskaya, A., Abt, D., Ahmed, I., Niemeyer, C. M., Barner-Kowollik, C., & Fruk, L. (2016). Photo-induced chemistry for the design of oligonucleotide conjugates and surfaces. Journal of Materials Chemistry B, 4(3), 442–449. https://doi.org/10.1039/c5tb02207j

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