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Sökning: id:"swepub:oai:DiVA.org:liu-114166" > Perturbation of DNA...

Perturbation of DNA hairpins containing the EcoRI recognition site by hairpin loops of varying size and composition : physical (NMR and UV) and enzymatic (EcoRI) studies

Germann, Markus W. (författare)
Departments of Biological Sciences, The University of Calgary Calgary, Alberta, Canada
Kalisch, Bernd W. (författare)
Medical Biochemistry, The University of Calgary Calgary, Alberta, Canada
Lundberg, Peter (författare)
Linköpings universitet,Avdelningen för radiologiska vetenskaper,Hälsouniversitetet,Centrum för medicinsk bildvetenskap och visualisering, CMIV,Region Östergötland, Radiofysikavdelningen US,Departments of Biological Sciences, The University of Calgary Calgary, Alberta, Canada
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Vogel, Hans J. (författare)
Departments of Biological Sciences, The University of Calgary Calgary, Alberta, Canada
van de Sande, Johan H. (författare)
Medical Biochemistry, The University of Calgary Calgary, Alberta, Canada
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 (creator_code:org_t)
Oxford University Press, 1990
1990
Engelska.
Ingår i: Nucleic Acids Research. - : Oxford University Press. - 0305-1048 .- 1362-4962. ; 18:6, s. 1489-1498
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We have investigated loop-induced structural perturbation of the stem structure in hairpins d(GAATTCXnGAATTC) (X = A, T and n = 3, 4, 5 and 6) that contain an EcoRI restriction site in close proximity to the hairpin loop. Oligonucleotides containing either a T3 or a A3 loop were not hydrolyzed by the restriction enzyme and also showed only weak binding to EcoRI in the absence of the cofactor Mg2+. In contrast, hairpins with larger loops are hydrolyzed by the enzyme at the scission site next to the loop although the substrate with a A4 loop is significantly more resistant than the oligonucleotide containing a T4 loop. The hairpin structures with 3 loop residues were found to be thermally most stable while larger hairpin loops resulted in structures with lower melting temperatures. The T-loop hairpins are thermally more stable than the hairpins containing the same number of A residues in the loop. As judged from proton NMR spectroscopy and the thermodynamic data, the base pair closest to the hairpin loop did form in all cases studied. The hairpin loops did, however, affect the conformation of the stem structure of the hairpins. From 31P and 1H NMR spectroscopy we conclude that the perturbation of the stem structure is stronger for smaller hairpin loops and that the extent of the perturbation is limited to 2-3 base pairs for hairpins with T3 or A4 loops. Our results demonstrate that hairpin loops modulate the conformation of the stem residues close to the loop and that this in turn reduces the substrate activity for DNA sequence specific proteins.

Ämnesord

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Nyckelord

*Dna
Deoxyribonuclease EcoRI/*metabolism
Electrophoresis
Polyacrylamide Gel
Magnesium/pharmacology
Magnetic Resonance Spectroscopy/methods
*Nucleic Acid Conformation
Nucleic Acid Denaturation
*Oligodeoxyribonucleotides/chemical synthesis
Spectrophotometry
Ultraviolet/methods
Substrate Specificity
Thermodynamics

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