Characterization of Nucleobase Analogue FRET Acceptor tCnitro
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Characterization of Nucleobase Analogue FRET Acceptor tCnitro. / Preus, Søren; Börjesson, Karl; Kilså, Kristine; Albinsson, Bo; Wilhelmsson, L. Marcus.
In: Journal of Physical Chemistry B, Vol. 114, No. 2, 2010, p. 1050-1056.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Characterization of Nucleobase Analogue FRET Acceptor tCnitro
AU - Preus, Søren
AU - Börjesson, Karl
AU - Kilså, Kristine
AU - Albinsson, Bo
AU - Wilhelmsson, L. Marcus
PY - 2010
Y1 - 2010
N2 - The fluorescent nucleobase analogues of the tricyclic cytosine (tC) family, tC and tCO, possess high fluorescence quantum yields and single fluorescence lifetimes, even after incorporation into double-stranded DNA, which make these base analogues particularly useful as fluorescence resonance energy transfer (FRET) probes. Recently, we reported the first all-nucleobase FRET pair consisting of tCO as the donor and the novel tCnitro as the acceptor. The rigid and well-defined position of this FRET pair inside the DNA double helix, and consequently excellent control of the orientation factor in the FRET efficiency, are very promising features for future studies of nucleic acid structures. Here, we provide the necessary spectroscopic and photophysical characterization of tCnitro needed in order to utilize this probe as a FRET acceptor in nucleic acids. The lowest energy absorption band from 375 to 525 nm is shown to be the result of a single in-plane polarized electronic transition oriented 27° from the molecular long axis. This band overlaps the emission bands of both tC and tCO, and the Frster characteristics of these donor-acceptor pairs are calculated for double-stranded DNA scenarios. In addition, the UV-vis absorption of tCnitro is monitored in a broad pH range and the neutral form is found to be totally predominant under physiological conditions with a pKa of 11.1. The structure and electronic spectrum of tCnitrois further characterized by density functional theory calculations.
AB - The fluorescent nucleobase analogues of the tricyclic cytosine (tC) family, tC and tCO, possess high fluorescence quantum yields and single fluorescence lifetimes, even after incorporation into double-stranded DNA, which make these base analogues particularly useful as fluorescence resonance energy transfer (FRET) probes. Recently, we reported the first all-nucleobase FRET pair consisting of tCO as the donor and the novel tCnitro as the acceptor. The rigid and well-defined position of this FRET pair inside the DNA double helix, and consequently excellent control of the orientation factor in the FRET efficiency, are very promising features for future studies of nucleic acid structures. Here, we provide the necessary spectroscopic and photophysical characterization of tCnitro needed in order to utilize this probe as a FRET acceptor in nucleic acids. The lowest energy absorption band from 375 to 525 nm is shown to be the result of a single in-plane polarized electronic transition oriented 27° from the molecular long axis. This band overlaps the emission bands of both tC and tCO, and the Frster characteristics of these donor-acceptor pairs are calculated for double-stranded DNA scenarios. In addition, the UV-vis absorption of tCnitro is monitored in a broad pH range and the neutral form is found to be totally predominant under physiological conditions with a pKa of 11.1. The structure and electronic spectrum of tCnitrois further characterized by density functional theory calculations.
KW - Faculty of Science
U2 - 10.1021/jp909471b
DO - 10.1021/jp909471b
M3 - Journal article
C2 - 20039634
VL - 114
SP - 1050
EP - 1056
JO - Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical
JF - Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical
SN - 1520-6106
IS - 2
ER -
ID: 17083927