WebSchematic description of the method. ( A) The DNA is shown as a 1D lattice of units numbered by index n, n = 1, …N.Protein binding to the m DNA units starting at unit n is characterized by the binding constant K n.Each unit is assigned the transfer matrix Q n which consists of statistical weights Q n ( i, j) giving the probabilities for unit n to be in … WebChemoradiation therapy (CRT), which combines a chemotherapeutic drug with ionizing radiation (IR), is the most common cancer treatment. At the molecular level, the binding of Pt-drugs to DNA sensitizes cancer cells to IR, mostly by increasing the damage induced by secondary low-energy (0–20 eV) electrons (LE Emerging concepts in nucleic acids: …
Chem-map profiles drug binding to chromatin in cells
WebThe proposed cooperative drug–DNA binding model has led to a hypothesis ( Shen et al., 1989c, 1990b) on the quinolone resistance mechanism that was found either in gyrA or gyrB. It states that any mutation which alters the configuration of the drug binding pocket on DNA could lead to drug resistance. Such a mutation is more likely to occur in ... WebAbstract. Significant progress has been made over the past few years in studies of drug-DNA interactions. Structure-based design strategies have yielded new DNA-binding … familienmitglied ist positiv
Drug--DNA interactions - PubMed
WebJul 1, 2001 · A flow linear dichroism technique is utilized to study the unwinding of supercoiled DNA induced by the binding of ethidium bromide (EB) and proflavine (PF) at different ratios r (drug added/DNA base). WebMar 6, 2024 · The current study investigated the promising anticancer drug 1,3,5-Tris(4-carboxyphenyl)benzene (H3BTB) against breast and cervical cancer cell lines. In addition, 1,3,5-Tris(4-carboxyphenyl)benzene binds to DNA by groove binding. The binding of H3BTB to DNA was found to be significant which unwinds the DNA helix. WebThe distamycin derivative FCE24517 binds both reversibly and irreversibly to DNA. At 37 degrees C, the drug originates reversible complexes that are strong enough to survive to the electrophoretic separation of the substrate. These complexes slowly evolve to covalent adducts (10(-4) adducts/bp/h) th … conwe oy