Literature DB >> 11999690

Fluorescence resonance energy transfer studies of U-shaped DNA molecules.

Mike Lorenz1, Alexander Hillisch, Stephan Diekmann.   

Abstract

Fluorescence resonance energy transfer studies allow to determine global shape properties of nucleic acids and nucleoprotein complexes. In many DNA-protein complexes, the DNA is more or less bent and the degree of bending can be obtained by FRET. For example, the DNA in complex with the integration host factor (IHF) is kinked by approximately 160 degrees building a U-shaped structure. The two DNA helix ends come close to one another in space in a distance range easily measurable by FRET. The global DNA structure of this complex can be mimicked by introducing two regions with unpaired bases ('bulges') into the DNA each producing a sharp kink of approximately 80 degrees. These U-shaped DNA constructs were used to measure the electrostatic interaction of the two nearly parallel negatively charged DNA helix arms. The electrostatic repulsion between the helix arms, and as a consequence their distance, decreases with growing salt concentration of mono- or divalent cations. This experimental approach also allows the sensitive study of the local structure of DNA sequences positioned between the two bulges.

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Year:  2002        PMID: 11999690     DOI: 10.1016/s1389-0352(01)00038-1

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  3 in total

1.  Flexible DNA bending in HU-DNA cocrystal structures.

Authors:  Kerren K Swinger; Kathryn M Lemberg; Ying Zhang; Phoebe A Rice
Journal:  EMBO J       Date:  2003-07-15       Impact factor: 11.598

2.  Structural confirmation of a bent and open model for the initiation complex of T7 RNA polymerase.

Authors:  Rosemary S Turingan; Cuihua Liu; Mary E Hawkins; Craig T Martin
Journal:  Biochemistry       Date:  2007-01-25       Impact factor: 3.162

3.  Pressure dissociation of integration host factor-DNA complexes reveals flexibility-dependent structural variation at the protein-DNA interface.

Authors:  Donald F Senear; Vira Tretyachenko-Ladokhina; Michael L Opel; Kimberly A Aeling; G Wesley Hatfield; Laurie M Franklin; Reuben C Darlington; J B Alexander Ross
Journal:  Nucleic Acids Res       Date:  2007-02-25       Impact factor: 16.971

  3 in total

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