Issue 3, 2016

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

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
22 Oct 2015
Accepted
01 Dec 2015
First published
01 Dec 2015
This article is Open Access
Creative Commons BY license

J. Mater. Chem. B, 2016,4, 442-449

Author version available

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

A. Vigovskaya, D. Abt, I. Ahmed, C. M. Niemeyer, C. Barner-Kowollik and L. Fruk, J. Mater. Chem. B, 2016, 4, 442 DOI: 10.1039/C5TB02207J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements