Hinge-helix formation and DNA bending in various lac repressor-operator complexes

C A Spronk, G E Folkers, A M Noordman, R Wechselberger, N van den Brink, R Boelens, R Kaptein

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The hinge-region of the lac repressor plays an important role in the models for induction and DNA looping in the lac operon. When lac repressor is bound to a tight-binding symmetric operator, this region forms an alpha-helix that induces bending of the operator. The presence of the hinge-helices is questioned by previous data that suggest that the repressor does not bend the wild-type operator. We show that in the wild-type complex the hinge-helices are formed and the DNA is bent, similar to the symmetric complex. Furthermore, our data show differences in the binding of the DNA binding domains to the half-sites of the wild-type operator and reveal the role of the central base-pair of the wild-type operator in the repressor-operator interaction. The differences in binding to the operator half-sites are incorporated into a model that explains the relative affinities of the repressor for various lac operator sequences that contain left and right half-sites with different spacer lengths.

Original languageEnglish
Pages (from-to)6472-80
Number of pages9
JournalEMBO Journal
Volume18
Issue number22
DOIs
Publication statusPublished - 15 Nov 1999

Keywords

  • Bacterial Proteins
  • Base Sequence
  • Cloning, Molecular
  • Escherichia coli Proteins
  • Lac Operon
  • Lac Repressors
  • Nuclear Magnetic Resonance, Biomolecular
  • Nucleic Acid Conformation
  • Oligodeoxyribonucleotides
  • Protein Conformation
  • Repressor Proteins

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