Literature DB >> 25236334

Modification of nucleic acids by azobenzene derivatives and their applications in biotechnology and nanotechnology.

Jing Li1, Xingyu Wang, Xingguo Liang.   

Abstract

Azobenzene has been widely used as a photoregulator due to its reversible photoisomerization, large structural change between E and Z isomers, high photoisomerization yield, and high chemical stability. On the other hand, some azobenzene derivatives can be used as universal quenchers for many fluorophores. Nucleic acid is a good candidate to be modified because it is not only the template of gene expression but also widely used for building well-organized nanostructures and nanodevices. Because the size and polarity distribution of the azobenzene molecule is similar to a nucleobase pair, the introduction of azobenzene into nucleic acids has been shown to be an ingenious molecular design for constructing light-switching biosystems or light-driven nanomachines. Here we review recent advances in azobenzene-modified nucleic acids and their applications for artificial regulation of gene expression and enzymatic reactions, construction of photoresponsive nanostructures and nanodevices, molecular beacons, as well as obtaining structural information using the introduced azobenzene as an internal probe. In particular, nucleic acids bearing multiple azobenzenes can be used as a novel artificial nanomaterial with merits of high sequence specificity, regular duplex structure, and high photoregulation efficiency. The combination of functional groups with biomolecules may further advance the development of chemical biotechnology and biomolecular engineering.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  DNA nanotechnology; azobenzene; nucleic acids; photoregulation; probes

Mesh:

Substances:

Year:  2014        PMID: 25236334     DOI: 10.1002/asia.201402758

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  3 in total

1.  Chromophoric Nucleoside Analogues: Synthesis and Characterization of 6-Aminouracil-Based Nucleodyes.

Authors:  Noam S Freeman; Curtis E Moore; L Marcus Wilhelmsson; Yitzhak Tor
Journal:  J Org Chem       Date:  2016-05-17       Impact factor: 4.354

2.  A study on endonuclease BspD6I and its stimulus-responsive switching by modified oligonucleotides.

Authors:  Liudmila A Abrosimova; Anzhela Yu Migur; Elena A Kubareva; Timofei S Zatsepin; Aleksandra V Gavshina; Alfiya K Yunusova; Tatiana A Perevyazova; Alfred Pingoud; Tatiana S Oretskaya
Journal:  PLoS One       Date:  2018-11-26       Impact factor: 3.240

3.  Azobenzene as a photoregulator covalently attached to RNA: a quantum mechanics/molecular mechanics-surface hopping dynamics study.

Authors:  Padmabati Mondal; Giovanni Granucci; Dominique Rastädter; Maurizio Persico; Irene Burghardt
Journal:  Chem Sci       Date:  2018-04-27       Impact factor: 9.825

  3 in total

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