Biophysics of knotting
Knots appear in a wide variety of biophysical systems, ranging from biopolymers, such as
DNA and proteins, to macroscopic objects, such as umbilical cords and catheters. Although …
DNA and proteins, to macroscopic objects, such as umbilical cords and catheters. Although …
Probability of DNA knotting and the effective diameter of the DNA double helix.
VV Rybenkov, NR Cozzarelli… - Proceedings of the …, 1993 - National Acad Sciences
During the random cyclization of long polymer chains, knots of different types are formed.
We investigated experimentally the distribution of knot types produced by random cyclization …
We investigated experimentally the distribution of knot types produced by random cyclization …
Analysis of the mechanism of DNA recombination using tangles
C Ernst, SJ Spengler, NR Cozzarelli - Quarterly reviews of …, 1995 - cambridge.org
The DNA of all organisms has a complex and essential topology. The three topological
properties of naturally occurring DNA are supercoiling, catenation, and knotting. Although …
properties of naturally occurring DNA are supercoiling, catenation, and knotting. Although …
The role of topoisomerase IV in partitioning bacterial replicons and the structure of catenated intermediates in DNA replication
DE Adams, EM Shekhtman, EL Zechiedrich… - Cell, 1992 - cell.com
Mutants in bacterial topoisomerase(topo) IV are deficient in chromosomal partitioning. To
investigate the basis of this phenotype, we examined plasmid DNA topology in conditionally …
investigate the basis of this phenotype, we examined plasmid DNA topology in conditionally …
RecQ helicase and topoisomerase III comprise a novel DNA strand passage function: a conserved mechanism for control of DNA recombination
FG Harmon, RJ DiGate, SC Kowalczykowski - Molecular cell, 1999 - cell.com
E. coli RecQ protein is a multifunctional helicase with homologs that include the S.
cerevisiae Sgs1 helicase and the H. sapiens Wrn and Blm helicases. Here we show that …
cerevisiae Sgs1 helicase and the H. sapiens Wrn and Blm helicases. Here we show that …
Thickness and crossing number of knots
G Buck, J Simon - Topology and its Applications, 1999 - Elsevier
Given a “short” piece of rope, one can tie only “simple” knots. We make this precise by
modeling “rope” as a solid tube of constant radius about a smooth core. The complexity of a …
modeling “rope” as a solid tube of constant radius about a smooth core. The complexity of a …
Topological selectivity in Xer site-specific recombination
SD Colloms, J Bath, DJ Sherratt - Cell, 1997 - cell.com
The product topology of Xer-mediated site-specific recombination at plasmid sites has been
determined. The product of deletion at pSC101 psi is a right-handed antiparallel 4-noded …
determined. The product of deletion at pSC101 psi is a right-handed antiparallel 4-noded …
Synthesizing topological structures containing RNA
Though knotting and entanglement have been observed in DNA and proteins, their
existence in RNA remains an enigma. Synthetic RNA topological structures are significant …
existence in RNA remains an enigma. Synthetic RNA topological structures are significant …
Monte Carlo analysis of the conformation of DNA catenanes
AV Vologodskii, NR Cozzarelli - Journal of molecular biology, 1993 - Elsevier
Abstract We used a Monte Carlo method to study the conformational properties of catenanes
between two nicked DNA rings. We calculated the writhe induced by catenation as a …
between two nicked DNA rings. We calculated the writhe induced by catenation as a …
The ColE1 unidirectional origin acts as a polar replication fork pausing site
E Viguera, P Hernández, DB Krimer, AS Boistov… - Journal of Biological …, 1996 - ASBMB
Co-orientation of replication origins is the most common organization found in nature for
multimeric plasmids. Streptococcus pyogenes broad-host-range plasmid pSM19035 and …
multimeric plasmids. Streptococcus pyogenes broad-host-range plasmid pSM19035 and …