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Göteborgs universitets publikationer

DNA adopts normal B-form upon incorporation of highly fluorescent DNA base analogue tC: NMR structure and UV-Vis spectroscopy characterization

Författare och institution:
Cecilia Engman (Institutionen för kemi); Peter Sandin (Institutionen för kemi och biovetenskap, Chalmers); Sadie Osborne (-); Tom Brown (-); Martin Billeter (Institutionen för kemi); Per Lincoln (Institutionen för kemi och biovetenskap, Chalmers); Bengt Nordén (Institutionen för kemi och biovetenskap, Chalmers); Bo Albinsson (Institutionen för kemi och biovetenskap, Chalmers); Marcus Wilhelmsson (Institutionen för kemi och biovetenskap, Chalmers)
Publicerad i:
Nucleic Acids Research, 32 ( 17 ) s. 5087-95
Artikel, refereegranskad vetenskaplig
Fulltextlänk (lokalt arkiv):
Sammanfattning (abstract):
The influence of the highly fluorescent tricyclic cytosine base analogue (tC) on duplex DNA conformation is investigated. The duplex properties are characterized by absorbance and circular dichroism (CD) for all combinations of neighbouring bases to tC, and an NMR structure is determined for one tC-containing sequence. For the oligonucleotides with one tC incorporated instead of cytosine, the melting temperature is increased on average by 2.7 degrees C above that for the unmodified ones. CD spectra are practically identical for modified and unmodified sequences, indicating an unperturbed B-DNA conformation. The NMR structure determination of the self-complementary sequence 5'-CTC(tC)ACGTGGAG shows a DNA conformation consistent with B-form for the whole duplex. The root-mean-square distance for the nucleotides of the eight central base pairs between the 10 structures with lowest CYANA target functions and a mean structure is 0.45 +/- 0.17 A. The NMR data confirm correct base pairing for tC by the observation of both intrastrand and interstrand imino proton NOEs. Altogether, this suggests that tC works well as a cytosine analogue, i.e. it is situated in the base stack, forming hydrogen bonds with G in the complementary strand, without distorting the DNA backbone conformation. This first example of an artificial, highly fluorescent DNA base that does not perturb the DNA conformation could have valuable applications for the study of the structure and dynamics of nucleic acid systems.
Ämne (baseras på Högskoleverkets indelning av forskningsämnen):
Kemi ->
Fysikalisk kemi ->
Biofysikalisk kemi
Kemi ->
Fysikalisk kemi ->
Biologiska vetenskaper ->
Biokemi och molekylärbiologi ->
Circular Dichroism, DNA, chemistry, Fluorescent Dyes, chemistry, Nuclear Magnetic Resonance, Biomolecular, Nucleic Acid Conformation, Phenothiazines, chemistry, Spectrophotometry, Spectrophotometry, Ultraviolet, Temperature
Chalmers styrkeområden:
Nanovetenskap och nanoteknik
Postens nummer:
Ingår i post nr:
Posten skapad:
2007-10-15 14:53
Posten ändrad:
2015-08-25 09:47

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