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      A highly homogeneous polymer composed of tetrahedron-like monomers for high-isotropy expansion microscopy

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          Abstract

          Expansion microscopy (ExM) physically magnifies biological specimens to enable nanoscale-resolution imaging on conventional microscopes. Current ExM methods permeate specimens with free-radical-chain-growth-polymerized polyacrylate hydrogels, whose network structure limits the local isotropy of expansion, and the preservation of morphology and shape at the nanoscale. Here we report that ExM is possible using hydrogels with more homogeneous network structure, assembled via non-radical terminal linking of tetrahedral monomers. As with earlier forms of ExM, such “tetra-gel”-embedded specimens can be iteratively expanded for greater physical magnification. Iterative tetra-gel expansion of HSV-1 virions by ~10x in linear dimension results in a median spatial error of 9.2 nm for localizing the viral envelope layer, rather than 14.3 nm from earlier versions of ExM. Moreover, tetra-gel-based expansion better preserved virion spherical shape. Thus, tetra-gels may support ExM with reduced spatial errors and improved local isotropy, pointing the way towards single biomolecule precision ExM.

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          Most cited references47

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          Optical imaging. Expansion microscopy.

          In optical microscopy, fine structural details are resolved by using refraction to magnify images of a specimen. We discovered that by synthesizing a swellable polymer network within a specimen, it can be physically expanded, resulting in physical magnification. By covalently anchoring specific labels located within the specimen directly to the polymer network, labels spaced closer than the optical diffraction limit can be isotropically separated and optically resolved, a process we call expansion microscopy (ExM). Thus, this process can be used to perform scalable superresolution microscopy with diffraction-limited microscopes. We demonstrate ExM with apparent ~70-nanometer lateral resolution in both cultured cells and brain tissue, performing three-color superresolution imaging of ~10(7) cubic micrometers of the mouse hippocampus with a conventional confocal microscope.
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            Design and Fabrication of a High-Strength Hydrogel with Ideally Homogeneous Network Structure from Tetrahedron-like Macromonomers

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              Imaging cellular ultrastructures using expansion microscopy (U-ExM)

              The attribution of a protein to an ultrastructural element by optical microscopy represents a major challenge in biology. Here, we report a method of near-native expansion microscopy (U-ExM), enabling the visualization of preserved ultrastructures of macromolecules by optical microscopy. Combined with super-resolution, U-ExM unveiled the centriolar chirality, only visualizable by electron microscopy. We demonstrate the general applicability of U-ExM by imaging different cellular structures including microtubules and mitochondria in cellulo.
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                Author and article information

                Journal
                101283273
                34218
                Nat Nanotechnol
                Nat Nanotechnol
                Nature nanotechnology
                1748-3387
                1748-3395
                1 March 2021
                29 March 2021
                June 2021
                29 September 2021
                : 16
                : 6
                : 698-707
                Affiliations
                [1 ]McGovern Institute for Brain Research, MIT, Cambridge, MA, USA.
                [2 ]Media Arts and Sciences, MIT, Cambridge, MA, USA.
                [3 ]Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
                [4 ]Department of Biological Engineering, MIT, MA, USA.
                [5 ]Broad Institute, MIT, Cambridge, MA, USA
                [6 ]Department of Neurology, Massachusetts General Hospital, Cambridge, MA, USA
                [7 ]Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA
                [8 ]Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
                [9 ]Program in Cellular and Molecular Medicine, Boston Children’s Hospital, Boston, MA, USA.
                [10 ]Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
                [11 ]Advanced Bioimaging Center, University of California at Berkeley, Berkeley, CA, USA
                [12 ]Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, CA, USA
                [13 ]MIT Center for Neurobiological Engineering, MIT, Cambridge, MA, USA.
                [14 ]Department of Brain and Cognitive Sciences, MIT, Cambridge, MA, USA.
                [15 ]Koch Institute, MIT, Cambridge, MA, USA.
                [16 ]Howard Hughes Medical Institute, Cambridge, MA, USA.
                [17 ]These authors contributed equally: Ruixuan Gao, Chih-Chieh (Jay) Yu
                Author notes

                Author contributions

                R.G. and L.G. designed and synthesized the monomers and conducted initial gelation experiments. C.-C.Y. and R.G. designed and conducted iterative expansion, virion expansion, and associated analysis. C.-C.Y. created the semi-automated virion analysis pipeline and the simulation model. K.D.P. helped characterization of the gel in cell culture. R.L.N. purified HSV-1 and prepared the virion stock solution. J.B.M. provided purified HIV virions. S.U. provided purified VSV virions and conducted initial virion immobilization experiments. C.-C.Y., R.G., and L.G. processed and performed quantitative analysis of all image data. R.G., C.-C.Y., and E.S.B. wrote the manuscript with input from all co-authors. E.S.B. supervised the project.

                Article
                NIHMS1673281
                10.1038/s41565-021-00875-7
                8197733
                33782587
                a7c15c0a-2c15-412c-8803-8ad7b4d8fb02

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                Nanotechnology
                Nanotechnology

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