The University of Southampton
University of Southampton Institutional Repository

Nucleic acid base analog fret-pair facilitating detailed structural measurements in nucleic acid containing systems

Nucleic acid base analog fret-pair facilitating detailed structural measurements in nucleic acid containing systems
Nucleic acid base analog fret-pair facilitating detailed structural measurements in nucleic acid containing systems
We present the first nucleobase analog fluorescence resonance energy transfer (FRET)-pair. The pair consists of tCO, 1,3-diaza-2-oxophenoxazine, as an energy donor and the newly developed tCnitro, 7-nitro-1,3-diaza-2-oxophenothiazine, as an energy acceptor.

The FRET-pair successfully monitors distances covering up to more than one turn of the DNA duplex. Importantly, we show that the rigid stacking of the two base analogs, and consequently excellent control of their exact positions and orientations, results in a high control of the orientation factor and hence very distinct FRET changes as the number of bases separating tCO and tCnitro is varied.

A set of DNA strands containing the FRET-pair at wisely chosen locations will, thus, make it possible to accurately distinguish distance- from orientation-changes using FRET.

In combination with the good nucleobase analog properties, this points toward detailed studies of the inherent dynamics of nucleic acid structures. Moreover, the placement of FRET-pair chromophores inside the base stack will be a great advantage in studies where other (biomacro)molecules interact with the nucleic acid.

Lastly, our study gives possibly the first truly solid experimental support to the dependence of energy transfer efficiency on orientation of involved transition dipoles as predicted by the Frster theory.
0002-7863
4288-4293
Börjesson, Karl
252a6cb2-9d9f-4e25-8e73-fad787fa8b8e
Preus, Søren
e2c84d70-23ea-4575-9fe7-1969fc931b68
El-Sagheer, Afaf H.
0bf56d90-78ee-4772-add8-453ccacc39be
Brown, Tom
a64aae36-bb30-42df-88a2-11be394e8c89
Albinsson, Bo
1571067f-df46-43f7-96b9-52dc43278777
Wilhelmsson, L. Marcus
bcf4f67a-198c-4c5e-80b8-a78f743509d4
Börjesson, Karl
252a6cb2-9d9f-4e25-8e73-fad787fa8b8e
Preus, Søren
e2c84d70-23ea-4575-9fe7-1969fc931b68
El-Sagheer, Afaf H.
0bf56d90-78ee-4772-add8-453ccacc39be
Brown, Tom
a64aae36-bb30-42df-88a2-11be394e8c89
Albinsson, Bo
1571067f-df46-43f7-96b9-52dc43278777
Wilhelmsson, L. Marcus
bcf4f67a-198c-4c5e-80b8-a78f743509d4

Börjesson, Karl, Preus, Søren, El-Sagheer, Afaf H., Brown, Tom, Albinsson, Bo and Wilhelmsson, L. Marcus (2009) Nucleic acid base analog fret-pair facilitating detailed structural measurements in nucleic acid containing systems. Journal of the American Chemical Society, 131 (12), 4288-4293. (doi:10.1021/ja806944w).

Record type: Article

Abstract

We present the first nucleobase analog fluorescence resonance energy transfer (FRET)-pair. The pair consists of tCO, 1,3-diaza-2-oxophenoxazine, as an energy donor and the newly developed tCnitro, 7-nitro-1,3-diaza-2-oxophenothiazine, as an energy acceptor.

The FRET-pair successfully monitors distances covering up to more than one turn of the DNA duplex. Importantly, we show that the rigid stacking of the two base analogs, and consequently excellent control of their exact positions and orientations, results in a high control of the orientation factor and hence very distinct FRET changes as the number of bases separating tCO and tCnitro is varied.

A set of DNA strands containing the FRET-pair at wisely chosen locations will, thus, make it possible to accurately distinguish distance- from orientation-changes using FRET.

In combination with the good nucleobase analog properties, this points toward detailed studies of the inherent dynamics of nucleic acid structures. Moreover, the placement of FRET-pair chromophores inside the base stack will be a great advantage in studies where other (biomacro)molecules interact with the nucleic acid.

Lastly, our study gives possibly the first truly solid experimental support to the dependence of energy transfer efficiency on orientation of involved transition dipoles as predicted by the Frster theory.

This record has no associated files available for download.

More information

Published date: 9 March 2009

Identifiers

Local EPrints ID: 146683
URI: http://eprints.soton.ac.uk/id/eprint/146683
ISSN: 0002-7863
PURE UUID: 9ae64beb-fddc-4bfd-95b7-ad90691427b2

Catalogue record

Date deposited: 22 Apr 2010 08:50
Last modified: 14 Mar 2024 00:56

Export record

Altmetrics

Contributors

Author: Karl Börjesson
Author: Søren Preus
Author: Afaf H. El-Sagheer
Author: Tom Brown
Author: Bo Albinsson
Author: L. Marcus Wilhelmsson

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×