Fluorescent RNA cytosine analogue - an internal probe for detailed structure and dynamics investigations.

Autor: Füchtbauer AF; Chemistry and Chemical Engineering/Chemistry and Biochemistry, Chalmers University of Technology, Gothenburg, SE-41296, Sweden., Preus S; Department of Chemistry, University of Copenhagen, Copenhagen, DK-2100, Denmark., Börjesson K; Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, SE-41296, Sweden., McPhee SA; Cancer Research UK Nucleic Acid Structure Research Group, MSI/WTB Complex, The University of Dundee, Dow Street, Dundee, DD1 5EH, UK., Lilley DMJ; Cancer Research UK Nucleic Acid Structure Research Group, MSI/WTB Complex, The University of Dundee, Dow Street, Dundee, DD1 5EH, UK., Wilhelmsson LM; Chemistry and Chemical Engineering/Chemistry and Biochemistry, Chalmers University of Technology, Gothenburg, SE-41296, Sweden. marcus.wilhelmsson@chalmers.se.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2017 May 24; Vol. 7 (1), pp. 2393. Date of Electronic Publication: 2017 May 24.
DOI: 10.1038/s41598-017-02453-1
Abstrakt: The bright fluorescent cytosine analogue tC O stands out among fluorescent bases due to its virtually unquenched fluorescence emission in duplex DNA. However, like most reported base analogues, it has not been thoroughly characterized in RNA. We here report on the first synthesis and RNA-incorporation of tC O , and characterize its base-mimicking and fluorescence properties in RNA. As in DNA, we find a high quantum yield inside RNA duplexes (<Φ F > = 0.22) that is virtually unaffected by the neighbouring bases (Φ F  = 0.20-0.25), resulting in an average brightness of 1900 M -1 cm -1 . The average fluorescence lifetime in RNA duplexes is 4.3 ns and generally two lifetimes are required to fit the exponential decays. Fluorescence properties in ssRNA are defined by a small increase in average quantum yield (<Φ F  > = 0.24) compared to dsRNA, with a broader distribution (Φ F  = 0.17-0.34) and slightly shorter average lifetimes. Using circular dichroism, we find that the tC O -modified RNA duplexes form regular A-form helices and in UV-melting experiments the stability of the duplexes is only slightly higher than that of the corresponding natural RNA (<ΔT m > = + 2.3 °C). These properties make tC O a highly interesting fluorescent RNA base analogue for detailed FRET-based structural measurements, as a bright internal label in microscopy, and for fluorescence anisotropy measurements of RNA dynamics.
Databáze: MEDLINE