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Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue

Bood, Mattias (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
Sandberg Wranne, Moa, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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Ro, J. J. (author)
Pohang University of Science and Technology
Sarangamath, Sangamesh, 1992 (author)
Chalmers tekniska högskola,Chalmers University of Technology,University of Edinburgh
El-Sagheer, A. H. (author)
Suez University
Rupert, Deborah, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Fisher, R. S. (author)
Magennis, S. W. (author)
University of Glasgow
Jones, A. C. (author)
University of Edinburgh
Höök, Fredrik, 1966 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Brown, T. (author)
University Of Oxford
Kim, B. H. (author)
Pohang University of Science and Technology
Dahlen, A. (author)
AstraZeneca AB
Wilhelmsson, Marcus, 1974 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Grötli, Morten (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
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 (creator_code:org_t)
2018
2018
English.
In: Chemical Science. - : Royal Society of Chemistry (RSC). - 2041-6520 .- 2041-6539. ; 9:14, s. 3494-3502
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Emissive base analogs are powerful tools for probing nucleic acids at the molecular level. Herein we describe the development and thorough characterization of pentacyclic adenine (pA), a versatile base analog with exceptional fluorescence properties. When incorporated into DNA, pA pairs selectively with thymine without perturbing the B-form structure and is among the brightest nucleobase analogs reported so far. Together with the recently established base analog acceptor qAnitro, pA allows accurate distance and orientation determination via Forster resonance energy transfer (FRET) measurements. The high brightness at emission wavelengths above 400 nm also makes it suitable for fluorescence microscopy, as demonstrated by imaging of single liposomal constructs coated with cholesterolanchored pA-dsDNA, using total internal reflection fluorescence microscopy. Finally, pA is also highly promising for two-photon excitation at 780 nm, with a brightness (5.3 GM) that is unprecedented for a base analog.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Fysik -- Atom- och molekylfysik och optik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Atom and Molecular Physics and Optics (hsv//eng)
NATURVETENSKAP  -- Fysik -- Annan fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Other Physics Topics (hsv//eng)
NATURVETENSKAP  -- Kemi -- Teoretisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Theoretical Chemistry (hsv//eng)

Keyword

pteridine nucleoside analogs
emissive rna alphabet
2-photon
excitation
nucleic-acid
quadracyclic adenine
nucleobase analogs
tc
2-aminopurine
nucleotides
environment

Publication and Content Type

ref (subject category)
art (subject category)

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