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 language | English |
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Pages (from-to) | 6472-80 |
Number of pages | 9 |
Journal | EMBO Journal |
Volume | 18 |
Issue number | 22 |
DOIs | |
Publication status | Published - 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