High-fold homogeneous expansion microscopy reveals structural details of centrioles and organelles, indicating improved resolution capabilities.
expansion while preserving cellular ultrastructure across diverse targets, including centrioles, nuclear pore complexes, and other organelles. hiHomoExM streamlines sample preparation and supports postexpansion labeling, allowing for both high labeling density and structural preservation. Furthermore, we extend the capability of hiHomoExM by integrating it into an iterative expansion framework to achieve even higher spatial resolution. Notably, coupling hiHomoEx with single-molecule localization microscopy (hiHomoEx-dSTORM) enables the resolution of previously elusive centriole ultrastructures, including the organization of CEP44, the microtubule-associated pattern of CCDC77, and the canonical 9-fold symmetry of SAS6. Together, hiHomoExM and hiHomoEx-dSTORM provide a robust and accessible platform for ∼2 nm-resolution characterization, bridging physical and optical super-resolution to advance cellular structural analysis.
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Yang et al. (2026) studied this question.
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