2026-09-19T05:20:25Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/1541622024-04-17T03:10:52Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022
Boyden, Edward S.
Shin, Tay Won
Program in Media Arts and Sciences (Massachusetts Institute of Technology)
2024-04-16T19:04:42Z
2024-04-16T19:04:42Z
2023-06
2023-08-16T20:34:30.481Z
https://hdl.handle.net/1721.1/154162
Neuroscientists have long studied complex neural circuits by examining their ultrastructure and molecular features. Electron microscopy (EM) has greatly advanced our fundamental understanding of neurobiology by revealing ultrastructural features through dense labeling of membranous structures while fluorescence microscopy (FM) allowed neuroscientists to identify and study specific biomolecules of interest. However, it would be ideal if such imaging could be achieved with FM (i.e., conventional light microscope), allowing anyone to identify and localize biomolecules in the detailed ultrastructural context of neural circuits. In this study, we report a novel membrane probe and modified expansion microscopy (ExM) protocol aimed at achieving conventional light microscope images that are comparable to low-resolution EM, enabling the visualization of ultrastructural features in thick mice brain tissue sections with molecular contrast, and pointing the way towards the possibility of tracing and reconstructing the neural circuitries. We demonstrate the ability of this novel strategy, which we call ultrastructure membrane expansion microscopy (umExM), to show ultrastructural features that were previously observable with EM using light microscopy and the localization of biomolecules in the ultrastructural context with a resolution of ~60 nm. Combining umExM with existing fluorescence fluctuation imaging methods (i.e., SRRF), we achieved a resolution of ~30 nm. umExM may enable the routine use of ultrastructure imaging in neurobiology.
Ph.D.
Massachusetts Institute of Technology
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https://rightsstatements.org/page/InC-EDU/1.0/
Scalable Chemical Tool for Analyzing Brain: Electron Microscope-Like Images with Fluorescent Microscope
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Doctor of Philosophy
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<Abstract>Neuroscientists have long studied complex neural circuits by examining their ultrastructure and molecular features. Electron microscopy (EM) has greatly advanced our fundamental understanding of neurobiology by revealing ultrastructural features through dense labeling of membranous structures while fluorescence microscopy (FM) allowed neuroscientists to identify and study specific biomolecules of interest. However, it would be ideal if such imaging could be achieved with FM (i.e., conventional light microscope), allowing anyone to identify and localize biomolecules in the detailed ultrastructural context of neural circuits. In this study, we report a novel membrane probe and modified expansion microscopy (ExM) protocol aimed at achieving conventional light microscope images that are comparable to low-resolution EM, enabling the visualization of ultrastructural features in thick mice brain tissue sections with molecular contrast, and pointing the way towards the possibility of tracing and reconstructing the neural circuitries. We demonstrate the ability of this novel strategy, which we call ultrastructure membrane expansion microscopy (umExM), to show ultrastructural features that were previously observable with EM using light microscopy and the localization of biomolecules in the ultrastructural context with a resolution of ~60 nm. Combining umExM with existing fluorescence fluctuation imaging methods (i.e., SRRF), we achieved a resolution of ~30 nm. umExM may enable the routine use of ultrastructure imaging in neurobiology.</Abstract>
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