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Getting DNA and RNA out of the dark with 2CNqA: a bright adenine analogue and interbase FRET donor

Wypijewska Del Nogal, Anna Wiktoria, 1982 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Füchtbauer, Anders (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,Chalmers tekniska högskola,Chalmers University of Technology,University of Gothenburg
Bood, Mattias (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg,AstraZeneca AB
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Nilsson, Jesper, 1984 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Sandberg Wranne, Moa, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Sarangamath, Sangamesh, 1992 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Pfeiffer, Pauline, 1994 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Sundar Rajan, Vinoth, 1987 (author)
Chalmers tekniska högskola,Chalmers University of Technology
El-Sagheer, A. H. (author)
Suez University
Dahlen, A. (author)
AstraZeneca AB
Brown, T. (author)
University Of Oxford
Grötli, Morten (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
Wilhelmsson, Marcus, 1974 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2020-06-19
2020
English.
In: Nucleic Acids Research. - : Oxford University Press (OUP). - 0305-1048 .- 1362-4962. ; 48:14, s. 7640-7652
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • With the central role of nucleic acids there is a need for development of fluorophores that facilitate the visualization of processes involving nucleic acids without perturbing their natural properties and behaviour. Here, we incorporate a new analogue of adenine, 2CNqA, into both DNA and RNA, and evaluate its nucleobase-mimicking and internal fluorophore capacities. We find that 2CNqA displays excellent photophysical properties in both nucleic acids, is highly specific for thymine/uracil, and maintains and slightly stabilises the canonical conformations of DNA and RNA duplexes. Moreover, the 2CNqA fluorophore has a quantum yield in single-stranded and duplex DNA ranging from 10% to 44% and 22% to 32%, respectively, and a slightly lower one (average 12%) inside duplex RNA. In combination with a comparatively strong molar absorptivity for this class of compounds, the resulting brightness of 2CNqA inside double-stranded DNA is the highest reported for a fluorescent base analogue. The high, relatively sequence-independent quantum yield in duplexes makes 2CNqA promising as a nucleic acid label and as an interbase Forster resonance energy transfer (FRET) donor. Finally, we report its excellent spectral overlap with the interbase FRET acceptors qA(nitro) and tC(nitro), and demonstrate that these FRET pairs enable conformation studies of DNA and RNA.

Subject headings

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

Keyword

quadracyclic adenine
ribosomal-subunit
nucleic-acid
fluorescence
tools
Biochemistry & Molecular Biology

Publication and Content Type

ref (subject category)
art (subject category)

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