ET DPHEN DNA · Electron transfer through multiple consecutive phenanthrenyl containing DNA
FP7 — People (Marie Curie Actions)
- Duration
- 2009-08-01 → 2011-07-31
- EU contribution
- €181,935
- Participants
- 1
- Scheme
- MC-IIF
Lines connect the coordinator with its partners.
Results in brief
Electron transfer through multiple consecutive phenanthrenyl containing DNA
This project had three interconnected goals aimed at improving our understanding of reductive electron transfer in DNA. Our first goal was to synthesise DNA containing aromatic nucleobase surrogates that can facilitate electron transfer in a DNA double helix. Next, we pursued the synthesis of electron donors with a higher reduction potential when compared to the aromatic nucleobase surrogates. Our last goal was to discover and design novel electron acceptors that can report on electron transfer by a fluorescent response. We have made progress in all three of the above research goals. We accomplished the synthesis of various pyrene and phenanthrene aromatic nucleobase surrogates that vary in their electron affinity. With respect to the electron donors we have synthesised phenothiazine and 1,5-diaminonapthalene electron donors that are compatible with oligonucleotide synthesis. Lastly, we designed and synthesised new electron acceptors that may report on electron transfer by a fluorescent response. The first generation electron acceptor was based on a well know highly fluorescent cytosine analogue. However, the substituted cytosine nucleobase did not produce any desired fluorescence quenching so we redesigned our approach for the discovery of these electron acceptors. Instead of substituting known fluorescent nucleobases with a fluorescence quencher and testing for fluorescence quenching we decided to conjugate fluorescent molecules that have previously shown to undergo quenching to the natural nucleobases. We attached a fluorescently quenched anthracene to deoxyuridine and indeed the quenching was preserved. In the future, the phenothiazine (PTZ) and 1,5-diaminonapthalene electron donors will be incorporated into DNA and tested for their ability to report on electron transfer by a fluorescent response. The above mentioned work will not only broaden our understanding of electron transfer through DNA but the combination of electron transfer with a fluorescence response may lead to new bioanalytical methods for detecting base mismatch and DNA damage.
Data: CORDIS, © European Union
Project objective
Synthesis and development of novel DNA base pairs that are orthogonal in their recognition properties compared to the natural base pairs are avidly pursued by scientists. Such novel base pairs are investigated as tools in biotechnology and in designing novel genetic systems. Interest in artificial base pairs continues because of their application in materials research and nanosciences. Likewise charge transfer (CT) through the DNA duplex has received considerable attention and is being explored in fundamental and applied research. The objective of this project is to synthesize and study DNA containing more than one phenanthrenyl-pair (dPhen-R) in a duplex DNA. This would provide the first example of electron transfer through a duplex containing multiple phenanthrenyl (dPhen-R) base replacements. Substitutions (R) on the ring will influence the redox potential of the aromatic system. This will also influence the electron transfer efficiency. This project will also pursue the synthesis of a base-pairing nucleobase analogue capable of acting as an electron acceptor. This electron acceptor will report on electron transfer by a fluorescent response and increase the stability of the duplex. The optimized DNA-based architecture will then be attached to a gold surface in order to observe direct electron transfer by nanoelectrochemistry. It is envisioned that this novel DNA architecture and future designs may be applied in DNA based biosensors and in the area of DNA nanomaterials.
Original text from CORDIS.
Participants
- UNIVERSITAET BERN · BernCoordinatorSwitzerland
Links
Data: CORDIS, © European Union
