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There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
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Ahmet F. Coskun, Ph.D.*
Instructor of Radiology
Stanford University School of Medicine
Monday, February 25, 2019
10:00 a.m. – 11:00 a.m.
Whitaker Building, 3115
Videoconference:
Emory: Health and Sciences Research Building, E160 Georgia Tech: TEP, stream from your PC (no conf. room) https://bluejeans.com/809850842
"Multiplex Imaging of Spatial Biology in Single Cells"
ABSTRACT
Spatial organization of cells and subcellular variations in tissues can be considered as a quantitative metric in determining the health and disease states. Single cell analyses of molecular profiles with in-situ detection methods dissect spatial heterogeneity of distinct cell types. Such detailed cellular maps shed light on spatial regulation mechanisms of diseases. In this talk, I will introduce multiplex imaging modalities to quantify up to hundred markers at macromolecular resolution in single cells. First, we have devised a “spatial genomics” method (seqFISH) to visualize 3D gene expression profiles in single cells. Using computational modeling of seqFISH data, we have formulated correlation FISH (corrFISH) to resolve dense RNA distributions in immune organs. CorrFISH identified cell-type specific gene expression of ribosomal proteins, a supporting evidence for specialized ribosome theory. Second, we have developed a “subcellular metabolomics” approach, Ion Beam Tomography (IBT), to quantify time-encoded 4D dynamics of chromatin, replication, and transcription at 65-nm lateral and 5-nm axial resolution. IBT revealed spatial segregation of transcription and replication in subcellular volumes of aberrant immune cells, a phase separation model for metabolic regulation of single cells. Lastly, we have demonstrated a “subcellular proteomics” scheme to determine 5D cancer-type specific profiles of nuclear markers in immune/cancer cells within archival patient samples. Super-resolved CODEX protein maps at 100-nm isotropic (x-y-z) resolution in FFPE tissues suggested spatial hierarchical ordering of epigenetics markers, intracellular signaling molecules, and cellular phenotypes in blood cancers. Together, image-based molecular profiling, when combined with advanced mathematical theories and computation, has the potential to decode high-dimensional dynamics at the subcellular and molecular level in complex tissues and organs. Automated machine learning algorithms in this single cell big data impact the biomedical practice and clinical care.
BIOGRAPHY
Dr. Coskun is currently an Instructor of Radiology at Stanford University School of Medicine. Dr. Coskun has been working with Prof. Garry Nolan as a faculty member at Stanford University. Dr. Coskun is an alumnus of the Ignite Entrepreneurship Program at the Stanford University Graduate School of Business. He is a recipient of the National Institutes of Health K25 Career Award (2018), the Burroughs Wellcome Fund CASI Award (2016), and the Leukemia & Lymphoma Research Fellowship (2015). Dr. Coskun previously trained at California Institute of Technology with Prof. Long Cai for his postdoctoral work in systems biology. He earned a Ph.D. degree in Electrical Engineering and Bioengineering (Minor) from the University of California, Los Angeles, working with Prof. Aydogan Ozcan. Dr. Coskun researches spatial biology, precision medicine, and biophotonics. His research centers on single cell analysis, subcellular imaging, and multiplex assays using interdisciplinary quantitative tools. Finally, Dr. Coskun promotes the use of Bioart and Nanoart for teaching, entrepreneurship in biotechnology, and Open Science to liberate scientific progress.
Host: Sakis Mantalaris
