Measurement of the contributions of 1D and 3D pathways to the translocation of a protein along DNA
- 21 October 2005
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 102 (44) , 15883-15888
- https://doi.org/10.1073/pnas.0505378102
Abstract
Proteins that act at specific DNA sequences bind DNA randomly and then translocate to the target site. The translocation is often ascribed to the protein sliding along the DNA while maintaining continuous contact with it. Proteins also can move on DNA by multiple cycles of dissociation/reassociation within the same chain. To distinguish these pathways, a strategy was developed to analyze protein motion between DNA sites. The strategy reveals whether the protein maintains contact with the DNA as it transfers from one site to another by sliding or whether it loses contact by a dissociation/reassociation step. In reactions at low salt, the test protein stayed on the DNA as it traveled between sites, but only when the sites were 30 bp at in vivo salt, and over distances of >50 bp at any salt, always included at least one dissociation step. Hence, for this enzyme, 1D sliding operates only over short distances at low salt, and 3D dissociation/reassociation is its main mode of translocation.Keywords
This publication has 38 references indexed in Scilit:
- Cleavage of Individual DNA Strands by the Different Subunits of the Heterodimeric Restriction Endonuclease BbvCIJournal of Molecular Biology, 2005
- Site-Specific DNA-nicking Mutants of the Heterodimeric Restriction Endonuclease R.BbvCIJournal of Molecular Biology, 2005
- Type II restriction endonucleases: structure and mechanismCellular and Molecular Life Sciences, 2005
- Origin recognition and the chromosome cycleFEBS Letters, 2004
- The energetics of the interaction of BamHI endonuclease with its recognition site GGATCC11Edited by R. EbrightJournal of Molecular Biology, 2001
- Anatomy of a preferred target site for the bacterial insertion sequence IS90311Edited by M. GottesmanJournal of Molecular Biology, 2001
- Divalent Metal Dependence of Site-Specific DNA Binding by EcoRV EndonucleaseBiochemistry, 1999
- DNA cleavage by the EcoRV restriction endonuclease: roles of divalent metal ions in specificity and catalysisJournal of Molecular Biology, 1999
- Diffusion-Controlled Macromolecular InteractionsAnnual Review of Biophysics, 1985
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985