Literature DB >> 15877339

Site-specific binding of the 9.5 kilodalton DNA-binding protein ORF80 visualized by atomic force microscopy.

M Lysetska1, H Zettl, I Oka, G Lipps, G Krauss, G Krausch.   

Abstract

Atomic force microscopy (AFM) has been used to examine the binding properties of the DNA-binding protein ORF80 to DNA. ORF80 is a 9.5 kDa protein that binds site-specifically to double-stranded DNA of the sequence TTAA-N(7)-TTAA. Direct sizing of the protein complexes on DNA fragments from the plasmid pRN1 with AFM shows that the protein ORF80 binds preferentially to two positions. These positions agree well with the ORF80 binding sites determined by footprinting analysis. The measurements allow an estimate of the stoichiometry of the DNA-protein complexes. In contrast to previous results, the single-molecule experiments suggest that only a low number of ORF80 molecules bind to a DNA-binding site.

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Year:  2005        PMID: 15877339     DOI: 10.1021/bm0494489

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  1 in total

1.  Structural and functional studies of Stf76 from the Sulfolobus islandicus plasmid-virus pSSVx: a novel peculiar member of the winged helix-turn-helix transcription factor family.

Authors:  Patrizia Contursi; Biancamaria Farina; Luciano Pirone; Salvatore Fusco; Luigi Russo; Simonetta Bartolucci; Roberto Fattorusso; Emilia Pedone
Journal:  Nucleic Acids Res       Date:  2014-03-25       Impact factor: 16.971

  1 in total

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