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Quadracyclic Adenin...
Quadracyclic Adenine: A Non-Perturbing Fluorescent Adenine Analogue
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- Dierckx, Anke, 1986 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Miannay, Francois-Alexandre, 1979 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Gaied, N. (author)
- University of Southampton
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- Preus, S. (author)
- Köpenhamns universitet,University of Copenhagen
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- Björck, Markus, 1987 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Brown, T. (author)
- University of Southampton
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- Wilhelmsson, Marcus, 1974 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
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(creator_code:org_t)
- 2012-03-21
- 2012
- English.
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In: Chemistry - A European Journal. - : Wiley. - 1521-3765 .- 0947-6539. ; 18:19, s. 5987-5997
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http://dx.doi.org/10...
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https://research.cha...
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https://doi.org/10.1...
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Abstract
Subject headings
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- Fluorescent-base analogues (FBAs) comprise a group of increasingly important molecules for the investigation of nucleic acid structure and dynamics as well as of interactions between nucleic acids and other molecules. Here, we report on the synthesis, detailed spectroscopic characterisation and base-pairing properties of a new environment-sensitive fluorescent adenine analogue, quadracyclic adenine (qA). After developing an efficient route of synthesis for the phosphoramidite of qA it was incorporated into DNA in high yield by using standard solid-phase synthesis procedures. In DNA qA serves as an adenine analogue that preserves the B-form and, in contrast to most currently available FBAs, maintains or even increases the stability of the duplex. We demonstrate that, unlike fluorescent adenine analogues, such as the most commonly used one, 2-aminopurine, and the recently developed triazole adenine, qA shows highly specific base-pairing with thymine. Moreover, qA has an absorption band outside the absorption of the natural nucleobases (>300 nm) and can thus be selectively excited. Upon excitation the qA monomer displays a fluorescence quantum yield of 6.8?% with an emission maximum at 456 nm. More importantly, upon incorporation into DNA the fluorescence of qA is significantly less quenched than most FBAs. This results in quantum yields that in some sequences reach values that are up to fourfold higher than maximum values reported for 2-aminopurine. To facilitate future utilisation of qA in biochemical and biophysical studies we investigated its fluorescence properties in greater detail and resolved its absorption band outside the DNA absorption region into distinct transition dipole moments. In conclusion, the unique combination of properties of qA make it a promising alternative to current fluorescent adenine analogues for future detailed studies of nucleic acid-containing systems.
Subject headings
- NATURVETENSKAP -- Kemi -- Fysikalisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Physical Chemistry (hsv//eng)
- NATURVETENSKAP -- Biologi -- Biofysik (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences -- Biophysics (hsv//eng)
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Keyword
- size-expanded dna
- dna-base analog
- DNA solid-phase synthesis
- binding
- peptide nucleic-acid
- 2-aminopurine
- pteridine nucleoside analogs
- oligonucleotides
- complex-formation
- duplexes
- fluorescence
- form
- duplex stability
- DNA
- fluorescent
Publication and Content Type
- art (subject category)
- ref (subject category)
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