Single-stranded-double-stranded DNA (ss-dsDNA) replication forks and primer-template junctions are important recognition sites for the assembly and function of proteins involved in DNA replication, recombination, and repair. DNA 'breathing' - i.e. thermally induced local fluctuations of the sugar-phosphate backbones and bases - can populate metastable conformational macrostates at positions near such junctions and likely play key roles in the functional interactions of the regulatory proteins that bind at these sites. Recently, Maurer et al. [1] performed polarization-sweep single-molecule fluorescence (PS-SMF) studies on exciton-coupled (iCy3)2 dimer-labeled ss-dsDNA fork constructs, which revealed that the nucleobases and backbones immediately adjacent to the dimer probes undergo conformational fluctuations on time scales ranging from hundreds of microseconds to hundreds of milliseconds. The local conformations sensed by the dimer probes consist of four quasi-stable macrostates whose populations and dynamics depend on dimer probe position relative to these junctions. Here we present theoretical analyses of these PS-SMF data that quantify the relative stabilities and activation barriers of the free energy surfaces of site-specific DNA 'breathing' events at key positions within these junctions. Our results suggest a detailed molecular picture for DNA 'breathing' at these positions, thus providing insights into understanding the molecular mechanisms of the proteins that operate at these sites.
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http://dx.doi.org/10.1093/nar/gkaf047 | DOI Listing |
Chem Asian J
March 2025
Birla Institute of Technology & Science Pilani - Hyderabad Campus, Chemistry, Jawaharnagar, Shamirpet Mandal, 500078, Hyderabad, INDIA.
In this work, we have investigated the metal sensing capabilities of dimeric fused heterocycles, PQ-BCN and PQN-BCN, bearing a pyrrole-pyridine chelating unit. PQ-BCN displayed selectivity towards Zn2+ in micromolar levels by steady-state absorbance and fluorescence-assisted screening experiments. The binding stoichiometry of the complex was determined to be a 2:1 metal-to-probe ratio, with an association constant (Ka) of 1.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2025
Universität Rostock, Institut für Chemie, Abteilung für Physikalische Chemie, Dr-Lorenz-Weg 2, Rostock 18059, Germany.
Ion pair formation is a fundamental concept in chemistry. The association between ions of opposite charge is widely used in synthesis and catalysis. In contrast, there is little evidence for the formation of cationic or anionic dimers in solution.
View Article and Find Full Text PDFLangmuir
March 2025
The MacDiarmid Institute for Advanced Materials and Nanotechnology, Victoria University of Wellington P.O. Box 600, Wellington 6040, New Zealand.
Thiolated DNA biopolymer probes are widely used for their spontaneous interactions with gold electrodes to achieve self-assembled monolayers (SAMs) of DNA. This offers an attractive class of bio-interfaces for developing point-of-care (POC) diagnostics. However, SAMs are prone to structural instability and can be challenging to reproducibly fabricate for probes of different sizes and shapes.
View Article and Find Full Text PDFSci Rep
March 2025
Department of Engineering Science, The University of Electro-Communications (UEC Tokyo), Chofu, Tokyo, 182-8585, Japan.
A method to simulate the dipole moment mode of the scanning nonlinear dielectric microscope (SNDM) has been developed. This method has been applied to the so-called [Formula: see text] dimer-adatom-stacking-fault (DAS) structure and a [Formula: see text] surface with one adatom and one restatom, which are the main motifs of the DAS structure. It has been revealed that a local upward dipole moment is observed at the adatom site, consistent with the SNDM experiments.
View Article and Find Full Text PDFBraftide, originally designed as a potent allosteric RAF kinase dimer disruptor, was intended to inhibit RAF dimerization by targeting the conserved RAF dimer interface. Intriguingly, Braftide has also been observed to trigger proteasome-mediated protein degradation with an unclear mechanism of action. This study elucidates the mechanism underlying Braftide's dual functionality and assesses its potential as a chemical probe to target kinase-chaperone interaction.
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