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Toward Complete Sequence Flexibility of Nucleic Acid Base Analogue FRET

Sandberg Wranne, Moa, 1986 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Füchtbauer, Anders Foller, 1984 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Dumat, Blaise, 1984 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
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Bood, Mattias (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg,AstraZeneca AB
El-Sagheer, A. H. (författare)
University Of Oxford,Suez University
Brown, T. (författare)
University Of Oxford
Gradén, Henrik, 1968 (författare)
AstraZeneca AB
Grötli, Morten (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,University of Gothenburg
Wilhelmsson, Marcus, 1974 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2017-06-27
2017
Engelska.
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 139:27, s. 9271-9280
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Forster resonance energy transfer (FRET) using fluorescent base analogues is a powerful means of obtaining high-resolution nucleic acid structure and dynamics information that favorably complements techniques such as NMR and X-ray crystallography. Here, we expand the base base FRET repertoire with an adenine analogue FRET-pair. Phosphoramidite-protected quadracyclic 2'-deoxyadenosine analogues qAN1 (donor) and qA(nitro) (acceptor) were synthesized and incorporated into DNA by a genetic, reliable, and high-yielding route, and both constitute excellent adenine analogues. The donor, qAN1, has quantum yields reaching 21% and 11% in single- and double-strands, respectively. To the best of our knowledge, this results in the highest average brightness of an adenine analogue inside DNA. Its potent emissive features overlap well with the absorption of qA(nitro), and thus enable accurate FRET-measurements over more than one turn of B-DNA. As we have shown previously for our cytosine analogue FRET-pair, FRET between qAN1 and qA(nitro) positioned at different base separations inside DNA results in efficiencies that are highly dependent on both distance and orientation. This facilitates significantly enhanced resolution in FRET structure determinations, demonstrated here in a study of conformational changes of DNA upon binding of the minor groove binder netropsin. Finally, we note that the donor and acceptor, of our cytosine FRET-pair, tC degrees and tC(nitro), can be conveniently combined with the acceptor and donor of our current adenine pair, respectively. Consequently, our base analogues can now measure base base FRET between 3 of the 10 possible base combinations and, through base-complementarity, between all sequence positions in a duplex.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Other Basic Medicine (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Nyckelord

FLUORESCENT ADENINE ANALOG
PTERIDINE NUCLEOSIDE ANALOGS
VERSATILE
PROTECTING GROUP
EMISSIVE RNA ALPHABET
SINGLE-MOLECULE FRET
QUADRACYCLIC ADENINE
CIRCULAR-DICHROISM
BUTYLDIMETHYLSILYLOXYMETHYL
GROUP
QUENCHING EFFICIENCIES
ENERGY-TRANSFER
Chemistry
Multidisciplinary
ATES OF AMERICA
V105
P18337
RYER L
1967
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF

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