Keynote Presentation: SuperResNET: Learning in-cell macromolecular architecture from SMLM data
Автор: Labroots
Загружено: 2025-12-10
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Presented By: Dr. Ivan Robert Nabi, PhD
Speaker Biography: Dr. Nabi is Professor and Director of Imaging in the Life Sciences Institute of the University of British Columbia in Vancouver, Canada with more than 30 years of cell biology experience in the field of cellular domains and their role in cancer progression and metastasis. His work focuses on: 1. the Gp78 ubiquitin ligase, defining its role as a regulator of ER-mitochondria contacts and showing that Gp78 basal mitophagy controls cancer cell ROS; and 2. functional and structural characterization of caveolin-1 domains, including caveolae and scaffolds. Recently, in collaboration with Dr. Ghassan Hamarneh (Computing Science, Simon Fraser University) he has actively developed AI-based analysis approaches for super-resolution microscopy.
Webinar: Keynote Presentation: SuperResNET: Learning in-cell macromolecular architecture from SMLM data w/ Live Q&A
Webinar Abstract: Protein structures are now being resolved at the atomic level, but deciphering their molecular organization in the cell remains a challenge. Super-resolution microscopy enables the use of fluorescent-based molecular localization tools to study molecular structure at the nanoscale level in the intact cell, bridging the mesoscale gap to classical structural biology methodologies. SuperResNET is an integrated machine learning-based analysis software for visualizing and quantifying 3D point cloud data acquired by single molecule localization microscopy (SMLM). The computational modules of SuperResNET include correction for multiple blinking of a single fluorophore, denoising, segmentation (clustering), and feature extraction, which are then used for cluster group identification, modularity analysis, blob retrieval and visualization in 2D and 3D. More recent updates to SuperResNET allow two-channel interaction distance analysis to determine how two proteins interact within macromolecular assemblies. SuperResNET can be effectively and easily applied to any SMLM event list from which it rapidly learns macromolecular architecture in the intact cell. I will describe the ability of network graph analysis software (SuperResNET) to determine molecular structure from dSTORM and MinFlux single molecule localization microscopy. Use cases to be described include molecular analysis of the nucleopore complex, structural changes to clathrin coated pits by inhibitors of clathrin endocytosis and the identification and structural characterization of caveolae and non-caveolar caveolin-1 scaffolds.
Learning Objectives:
1. Explain how SMLM breaks the diffraction barrier
2. Compare structure determination by SuperResNET to that obtained by cryoEM
3. Describe the structure and function of Cav1 scaffolds and caveolae
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