BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20250626T121328EDT-2183OvoUr6@132.216.98.100 DTSTAMP:20250626T161328Z DESCRIPTION:How macromolecules behave in nanoconfined spaces\, such as what conformations DNA polymers adopt and how they interact with other DNA and protein molecules\, is of immense fundamental as well as applied interest \, warranting new biophysical explorations. In the context of cellular bio physics\, compact coiled DNA molecules are squeezed within a nucleus\, pre senting open questions regarding their properties and interactions. In the context of genomics\, nanofluidic tools often work by squeezing polymers into long nano pipes\, with the hope of directly unraveling the sequence o f our genetic code\, using small numbers of intact DNA segments. One holy grail of modern biotechnology is reading\, assembling and understanding si ngle-cell genomes with minimal fragmentation. However\, handling and visua lizing long and delicate strands of genomic DNA represent key technologica l challenges\, typically breaking DNA into tiny pieces.\n\nIn this talk\, we harness capabilities of a novel single-molecule manipulation and micros copy platform we have developed called “Convex Lens-induced Confinement (C LiC)” for two explorations in biophysics. First\, we demonstrate a new and gentle approach to directly manipulate and visualize long\, purified stra nds of DNA for genomic analysis which is high-throughput\, compatible with in-situ reagent exchange and controlled chemistry in nanofluidic environm ents\, and relies on tiny entropic forces (Berard et al\, PNAS 2014). We p recisely explore the polymer physics underlying the DNA polymers’ behaviou r as a function of applied confinement\, and compare results to theory\, w hich we consequently extend. Second\, using more complex supercoiled DNA s ystems\, closer to physiological conditions\, we study how their conformat ional fluctuations mediate invasion into spontaneous unwinding sites by sm all oligonucleotides. Motivated by open questions on transcriptional initi ation and dynamics\, and beginning with model systems\, our single-molecul e reaction and trajectory visualizations can provide new mechanistic insig hts. The overarching vision of this talk is that by “getting into that roo m at the bottom” of nanobiophysics by innovative technologies\, we open do ors to complementary biophysical discovery and biomedical diagnostics whic h can act hand in hand.\n DTSTART:20160126T180000Z DTEND:20160126T193000Z LOCATION:Rm 10\, Maass Chemistry Building\, CA\, QC\, Montreal\, H3A 0B8\, 801 rue Sherbrooke Ouest SUMMARY:Chemical Society Seminar: Dr. Sabrina Leslie URL:/chemistry/channels/event/chemical-society-seminar -dr-sabrina-leslie-257562 END:VEVENT END:VCALENDAR