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Development of bright fluorescent quadracyclic adenine analogues: TDDFT-calculation supported rational design

Larsen, Anders Foller, 1984 (author)
Dumat, Blaise, 1984 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Sandberg Wranne, Moa, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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Lawson, Christopher, 1968 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
Preus, S. (author)
Århus Universitet,Aarhus University
Bood, Mattias (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
Gradén, Henrik, 1968 (author)
AstraZeneca AB
Wilhelmsson, Marcus, 1974 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Grøtli, Morten, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
Füchtbauer, Anders Foller, 1984 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2015-07-31
2015
English.
In: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Fluorescent base analogues (FBAs) comprise a family of increasingly important molecules for the investigation of nucleic acid structure and dynamics. We recently reported the quantum chemical calculation supported development of four microenvironment sensitive analogues of the quadracyclic adenine (qA) scaffold, the qANs, with highly promising absorptive and fluorescence properties that were very well predicted by TDDFT calculations. Herein, we report on the efficient synthesis, experimental and theoretical characterization of nine novel quadracyclic adenine derivatives. The brightest derivative, 2-CNqA, displays a 13-fold increased brightness (epsilon Phi(F) = 4500) compared with the parent compound qA and has the additional benefit of being a virtually microenvironment-insensitive fluorophore, making it a suitable candidate for nucleic acid incorporation and use in quantitative FRET and anisotropy experiments. TDDFT calculations, conducted on the nine novel qAs a posteriori, successfully describe the relative fluorescence quantum yield and brightness of all qA derivatives. This observation suggests that the TDDFT-based rational design strategy may be employed for the development of bright fluorophores built up from a common scaffold to reduce the otherwise costly and time-consuming screening process usually required to obtain useful and bright FBAs.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Nucleic-Acid
Photophysical Properties
Cytosine Analog
Base Analog
Pyrrolo-Dc
Nucleoside
Density
Oligonucleotides
Probes
Fluorophore
Fluorophore

Publication and Content Type

ref (subject category)
art (subject category)

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