Literature DB >> 9356247

Affinity and specificity of trp repressor-DNA interactions studied with fluorescent oligonucleotides.

R J Reedstrom1, M P Brown, A Grillo, D Roen, C A Royer.   

Abstract

Fluorescence-based solution methods have been used to study the binding of the trp repressor of Escherichia coli to a series of oligonucleotides bearing all or partial determinants for high affinity specific binding. The tryptophan, salt concentration and competitor DNA dependence of the binding affinities was examined for these targets. Binding to a fluorescein-labeled 20 base-pair hairpin structure oligonucleotide, which contains a palindromic repressor binding site (GAACTAGTTAACTAGTAC) and is known to bind repressor in a 1 : 1 dimer-DNA complex, resulted in a protein concentration-dependent, competable static quenching of fluorescence in presence of co-repressor, l-tryptophan. The affinity recovered from the fits of these intensity profiles at 100 mM KCl was on the order of 4x10(8) M-1. In absence of co-repressor an increase in intensity at high repressor concentration (>10(-7) M) was observed. The salt concentration dependence of the specific binding of the holo-repressor to this oligonucleotide was approximately half as large as what would be predicted by the number of phosphate contacts in the crystal structures of the complex. Repressor binding to the fluorescein-labeled hairpin 20mer was compared with binding to a rhodamine-labeled 36 base-pair oligonucleotide bearing two inverted structural half-sites GNACT separated by an eight base-pair spacer containing none of the natural intervening sequence. The rather low affinity observed for the 36mer revealed that the intervening sequence in the natural operators contains energetic specificity determinants. Binding to a rhodamine-labeled oligonucleotide bearing a completely non-specific sequence was shown to occur over the same concentration range (>100 nM), regardless of tryptophan concentration, whereas binding to sequences bearing partial specificity ratio between 100 and 1000, depending upon the salt concentration. Even in absence of added KCl, the specificity ratio of trp repressor was greater than 100, implicating a significant free energy contribution from non-electrostatic interaction forces. Copyright 1997 Academic Press Limited.

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Year:  1997        PMID: 9356247     DOI: 10.1006/jmbi.1997.1333

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  9 in total

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Authors:  Michael M Hoffman; Maksim A Khrapov; J Colin Cox; Jianchao Yao; Lingnan Tong; Andrew D Ellington
Journal:  Nucleic Acids Res       Date:  2004-01-01       Impact factor: 16.971

2.  Surface plasmon resonance studies of wild-type and AV77 tryptophan repressor resolve ambiguities in super-repressor activity.

Authors:  Michael D Finucane; Oleg Jardetzky
Journal:  Protein Sci       Date:  2003-08       Impact factor: 6.725

3.  The Tumbleweed: towards a synthetic proteinmotor.

Authors:  Elizabeth H C Bromley; Nathan J Kuwada; Martin J Zuckermann; Roberta Donadini; Laleh Samii; Gerhard A Blab; Gregory J Gemmen; Benjamin J Lopez; Paul M G Curmi; Nancy R Forde; Derek N Woolfson; Heiner Linke
Journal:  HFSP J       Date:  2009-04-28

4.  Fluorescence recovery assay for the detection of protein-DNA binding.

Authors:  Xiaoyang Xu; Zhen Zhao; Lidong Qin; Wei Wei; Jon E Levine; Chad A Mirkin
Journal:  Anal Chem       Date:  2008-05-23       Impact factor: 6.986

5.  DNA binding and oligomerization of NtrC studied by fluorescence anisotropy and fluorescence correlation spectroscopy.

Authors:  F W Sevenich; J Langowski; V Weiss; K Rippe
Journal:  Nucleic Acids Res       Date:  1998-03-15       Impact factor: 16.971

6.  Probing the role of water in the tryptophan repressor-operator complex.

Authors:  M P Brown; A O Grillo; M Boyer; C A Royer
Journal:  Protein Sci       Date:  1999-06       Impact factor: 6.725

7.  Binding affinity of Escherichia coli RNA polymerase*sigma54 holoenzyme for the glnAp2, nifH and nifL promoters.

Authors:  Sabine K Vogel; Alexandra Schulz; Karsten Rippe
Journal:  Nucleic Acids Res       Date:  2002-09-15       Impact factor: 16.971

8.  Visualization of trp repressor and its complexes with DNA by atomic force microscopy.

Authors:  E Margeat; C Le Grimellec; C A Royer
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

9.  Switching DNA-binding specificity by unnatural amino acid substitution.

Authors:  Atanu Maiti; Siddhartha Roy
Journal:  Nucleic Acids Res       Date:  2005-10-13       Impact factor: 16.971

  9 in total

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