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Visualizing proteins by expansion microscopy

Abstract

Fluorescence imaging is one of the most versatile and widely-used tools in biology 1 . Although techniques to overcome the diffraction barrier were introduced more than two decades ago, and the nominal attainable resolution kept improving 2, 3 , fluorescence microscopy still fails to image the morphology of single proteins or small molecular complexes, either purified or in a cellular context 4, 5 . Here we report a solution to this problem, in the form of o ne-step n anoscale e xpansion (ONE) microscopy. We combined the 10-fold axial expansion of the specimen (1000-fold by volume) with a fluorescence fluctuation analysis 6, 7 to enable the description of cultured cells, tissues, viral particles, molecular complexes and single proteins. At the cellular level, using immunostaining, our technology revealed detailed nanoscale arrangements of synaptic proteins, including a quasi-regular organisation of PSD95 clusters. At the single molecule level, upon main chain fluorescent labelling, we could visualise the shape of individual membrane and soluble proteins. Moreover, conformational changes undergone by the ∼17 kDa protein calmodulin upon Ca 2+ binding were readily observable. We also imaged and classified molecular aggregates in cerebrospinal fluid samples from Parkinson’s Disease (PD) patients, which represents a promising new development towards improved PD diagnosis. ONE microscopy is compatible with conventional microscopes and can be performed with the software we provide here as a free, open-source package. This technology bridges the gap between high-resolution structural biology techniques and light microscopy, and provides a new avenue for discoveries in biology and medicine.

Authors

Ali Shaib, Abed Alrahman Chouaib, Rajdeep Chowdhury, Daniel Mihaylov, Chi Zhang, Vanessa Imani, Svilen V Georgiev, Nikolaos Mougios, Mehar Monga, Sofiia Reshetniak, Tiago Mimoso, Han Chen, Parisa Fatehbasharzad, Dagmar Crzan, Kim-Ann Saal, Nadia Alawar, Janna Eilts, Jinyoung Kang, Luis Alvarez, Claudia Trenkwalder, Brit Mollenhauer, Tiago Fleming Outeiro, Sarah Köster, Julia Preobraschenski, Ute Becherer, Tobias Moser, Edward Boyden, Radu Aricescu, Markus Sauer, Felipe Opazo, Silvio O Rizzoli

University Medical Center Goettingen

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45 products referenced in this preprint paper

(104 211) Synaptobrevin2

an Antibody by Synaptic Systems

(105 011) Synaptotagmin1

an Antibody by Synaptic Systems

Applications:

ICC-IF

(105 311) Synaptotagmin1

an Antibody by Synaptic Systems

Reactivity:

Rattus norvegicus (Rat)

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Preprint

Preprint Server BioRxiv : the Preprint Server for Biology

Publication Date 5 August 2022

View on EPMC

Publication metadata is provided by Europe PMC®, a database led by EMBL-EBI. Information for this publication was last updated on 2025-08-27 22:11:28 UTC.

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