Event | Date and Location | Summary |
Luis Ortiz-Rodriguez (University of Michigan) | Wed. November 20th, 2024 4:30 pm-5:30 pm at Clapp 108 |
Biomolecular Condensation Enables Material State Changes that Dynamically Regulate RNA Metabolism Recently, biomolecular condensates have emerged as a broadly utilized mechanism for organizing biochemical pathways within cells, and this organizational paradigm is particularly important within bacteria because these organisms generally lack membrane-bound organelles. Bacterial ribonucleoprotein bodies (BR-bodies) are dynamic biomolecular condensates that play a pivotal role in bacterial RNA metabolism. In this talk, I will demonstrate how BR-bodies orchestrate mRNA decay and storage based on a multidisciplinary approach that combines single-molecule fluorescence microscopy, bulk imaging techniques, biochemical assays, and rigorous quantitative analyses. During exponential growth, BR-bodies act as fluid-like condensates that enhance mRNA decay. Continue reading… Luis Ortiz-Rodriguez (University of Michigan) |
Event | Date | Summary |
Luis Ortiz-Rodriguez (University of Michigan) | Wed. November 20th, 2024 4:30 pm-5:30 pm |
Biomolecular Condensation Enables Material State Changes that Dynamically Regulate RNA Metabolism Recently, biomolecular condensates have emerged as a broadly utilized mechanism for organizing biochemical pathways within cells, and this organizational paradigm is particularly important within bacteria because these organisms generally lack membrane-bound organelles. Bacterial ribonucleoprotein bodies (BR-bodies) are dynamic biomolecular condensates that play a pivotal role in bacterial RNA metabolism. In this talk, I will demonstrate how BR-bodies orchestrate mRNA decay and storage based on a multidisciplinary approach that combines single-molecule fluorescence microscopy, bulk imaging techniques, biochemical assays, and rigorous quantitative analyses. During exponential growth, BR-bodies act as fluid-like condensates that enhance mRNA decay. Continue reading… Luis Ortiz-Rodriguez (University of Michigan) |
Rengasayee Veeraraghavan – Ohio State | Wed. November 6th, 2024 4:30 pm-5:30 pm |
Rapid, Hyperparameter-free Point Pattern Analysis of Single Molecule Localizations in 3D using Voronoi Tessellation-Based Clustering Growing evidence indicates that cardiac biology and physiology at cellular through organ scales are governed by the action of proteins organized within nanodomains with specialized ultrastructural properties. Multiple phenomena have been identified, whose function and dysfunction cannot be predicted without accounting for the makeup and behavior of nanodomains. Thus, my laboratory’s investigative approach is grounded in high resolution structural and functional imaging, complemented by our development of novel imaging and image analysis approaches. I will present work illustrating how super-resolution microscopy and quantitative image analysis have enabled us to make inroads into cardiac physiology, |
Clarice D. Aiello (UCLA, Quantum Biology Tech (QuBiT) Lab) | Tue. October 3rd, 2023 1:00 pm-2:00 pm |
PLEASE NOTE SPECIAL TIME/LOCATION “Quantum Biology”: how nature harnesses quantum processes to function optimally, and how might we control such quantum processes to therapeutic and tech advantage Imagine driving cell activities to treat injuries and disease simply by using tailored magnetic fields. Many relevant physiological processes, such as: the regulation of oxidative stress, proliferation, and respiration rates in cells; wound healing; ion channel functioning; and DNA repair were all demonstrated to be controlled by weak magnetic fields (with a strength on the order of that produced by your cell phone). Continue reading… Clarice D. Aiello (UCLA, Quantum Biology Tech (QuBiT) Lab) |
Thorsten Schmidt (Kent State University) | Wed. December 7th, 2022 4:30 pm-5:30 pm |
DNA Nanotechnology Tools for Single-Molecule Cryo-EM of Membrane Proteins DNA is a unique polymer. It is the information storage molecule of all known life forms, but can also be used to build up complex, artificial structures that are not found in Biology. Our group is leveraging this programmability to engineer nanoscale architectures and tools for applications in Biophysics and Structural Biology. I will demonstrate how DNA-lipid nanodiscs1 can be made and used as novel molecular tools to study membrane proteins (MPs) in a native membrane-like environment. MPs are key players in cellular functions such as sensing, |
Sebastian Sensale (Cleveland State University) | Wed. November 16th, 2022 4:30 pm-5:30 pm |
Title: Dynamic DNA Nanotechnology Sebastian Sensale Rodriguez Assistant Professor Abstract: Taking inspiration from macroscopic machines, the last decade has seen a surge of interest in the development of DNA origami devices whose functions heavily rely on conformational changes. These “dynamic” DNA nanodevices have found application in diverse areas of research including drug delivery, molecular computation, nanorobotics and biosensing. While the design, modeling and characterization of macroscopic machines is well determined on the basis of kinematics and continuum mechanics, the intrinsic flexibility and stochastic nature of biological systems at the nanoscale make such tasks be highly challenging. Continue reading… Sebastian Sensale (Cleveland State University) |
Divita Mathur (CWRU) | Wed. November 2nd, 2022 4:30 pm-5:30 pm |
Updated Zoom Link!!! https://cwru.zoom.us/j/92624627629?pwd=YnNLU2wzL0svRzEzaU9sY24zRklqZz09 Meeting ID: 926 2462 7629
Title: Synthetic DNA Nanostructures as Platforms for Precise Nanoparticle Organization |
Thereza Soares (Federal Univ. of Pernambuco) | Wed. April 6th, 2022 4:30 pm-5:30 pm |
POSTPONED due to COVID Continue reading… Thereza Soares (Federal Univ. of Pernambuco) |
Chitra Nayak (Tuskegee University) | Wed. October 6th, 2021 4:30 pm-5:30 pm |
Biological signals and cell signaling pathways – A computational approach. Type I interferons are used effectively in the treatment of Hepatitis C by activating a cascade of interferon-stimulated genes with antiviral properties. The signaling cascade involves the binding of IFN to the two subunits of the IFN receptor, IFNAR1 (R1) and IFNAR2 (R2), to form a ternary complex. The kinases – Jak’s and Tyk’s – bound to the cytoplasmic domains of receptor subunits become phosphorylated, which further phosphorylates STAT (p-STAT). Dimers of p-STAT migrate to the nucleus to initiate the transcription of a large number of genes. |
Jianhua Xing (University of Pittsburgh) | Wed. December 2nd, 2020 4:30 pm-5:30 pm |
Reconstructing cell phenotypic transition dynamics from single cell data Recent advances in single-cell techniques catalyze an emerging field of studying how cells convert from one phenotype to another, i.e., cell phenotypic transitions (CPTs). Two grand technical challenges, however, impede further development of the field. Fixed cell-based approaches can provide snapshots of high-dimensional expression profiles but have fundamental limits on revealing temporal information, and fluorescence-based live cell imaging approaches provide temporal information but are technically challenging for multiplex long- term imaging. My lab is tackling these grand challenges from two directions, with the ultimate goal of integrating the two directions to reconstruct the spatial-temporal dynamics of CPTs. |
Roberto Carlos Andresen Eguiluz (UC Merced) | Wed. November 11th, 2020 4:30 pm-5:30 pm |
On the quest of finding the surface of articular cartilage The primary role of articular cartilage (AC) is to provide a smooth lubricated surface between contacting and moving bones, which allows for ultralow friction as well as wear protection to the sliding epiphysis for almost a century in healthy people. The physical and chemical nature of the topmost surface of AC has intrigued researchers since it was first reported in 1951, called the “lamina splendens”. This layer has been the source of heated and controversial scientific debate since it was first reported. The lamina splendens is important because it forms the interfaces between the cartilage and synovial fluid, Continue reading… Roberto Carlos Andresen Eguiluz (UC Merced) |
Caitlin Davis (Yale University) | Wed. October 14th, 2020 4:30 pm-5:30 pm |
Title: Protein dynamics: Connecting in vitro, in cell, and in vivo Although biomolecules evolved to function in the cell, most biochemical and biophysical studies have been carried out in vitro. A combination of in vitro, in-cell, and in vivo studies will highlight how steric and non-steric interactions modulate protein folding and protein-RNA interactions. I will introduce a customized pipeline that combines meganuclease mediated transformation with fluorescence-detected temperature-jump microscopy to image fast dynamics of biomolecules in living zebrafish with single-cell resolution. To interpret in vivo and in-cell results, an in vitro systematic series of solvation environments will distinguish contributions from non-steric and steric interactions to stability, |
Jessica Winter (Ohio State University) | Wed. February 5th, 2020 4:30 pm-5:30 pm |
Twenty Years Later: Why No Clinical Quantum Dot Imaging Labels? Quantum dots (QDs), semiconductor nanoparticles that fluoresce upon light excitation, were first |
Kevin Wood (University of Michigan) | Wed. January 22nd, 2020 4:30 pm-5:30 pm |
Emergence and control in microbial communities: steering bacterial pathogens through the phenotype space of multidrug resistance Antibiotic resistance is a growing public health threat. The emergence of resistance far outpaces the development of new drugs, underscoring the need for new strategies aimed at slowing the resistance threat. In this talk, I’ll discuss our group’s ongoing work to understand the evolution of drug resistance in E. faecalis, an opportunistic bacterial pathogen, using quantitative experiments and theoretical tools from statistical physics and dynamical systems. By combining laboratory evolution with simple mathematical models, we show that unconventional strategies–including aperiodic drug dosing, |