High-fidelity 3D live-cell nanoscopy through data-driven enhanced super-resolution radial fluctuation

dc.contributor.authorLaine R.F.
dc.contributor.authorHeil H.S.
dc.contributor.authorCoelho S.
dc.contributor.authorNixon-Abell J.
dc.contributor.authorJimenez A.
dc.contributor.authorWiesner T.
dc.contributor.authorMartínez D.
dc.contributor.authorGalgani T.
dc.contributor.authorRégnier L.
dc.contributor.authorStubb A.
dc.contributor.authorFollain G.
dc.contributor.authorWebster S.
dc.contributor.authorGoyette J.
dc.contributor.authorDauphin A.
dc.contributor.authorSalles A.
dc.contributor.authorCulley S.
dc.contributor.authorJacquemet G.
dc.contributor.authorHajj B.
dc.contributor.authorLeterrier C.
dc.contributor.authorHenriques R.
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.converis.publication-id181714556
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/181714556
dc.date.accessioned2025-08-28T01:40:58Z
dc.date.available2025-08-28T01:40:58Z
dc.description.abstract<p>Live-cell super-resolution microscopy enables the imaging of biological structure dynamics below the diffraction limit. Here we present enhanced super-resolution radial fluctuations (eSRRF), substantially improving image fidelity and resolution compared to the original SRRF method. eSRRF incorporates automated parameter optimization based on the data itself, giving insight into the trade-off between resolution and fidelity. We demonstrate eSRRF across a range of imaging modalities and biological systems. Notably, we extend eSRRF to three dimensions by combining it with multifocus microscopy. This realizes live-cell volumetric super-resolution imaging with an acquisition speed of ~1 volume per second. eSRRF provides an accessible super-resolution approach, maximizing information extraction across varied experimental conditions while minimizing artifacts. Its optimal parameter prediction strategy is generalizable, moving toward unbiased and optimized analyses in super-resolution microscopy.<br></p>
dc.identifier.eissn1548-7105
dc.identifier.jour-issn1548-7091
dc.identifier.olddbid207883
dc.identifier.oldhandle10024/190910
dc.identifier.urihttps://www.utupub.fi/handle/11111/54564
dc.identifier.urlhttps://www.nature.com/articles/s41592-023-02057-w
dc.identifier.urnURN:NBN:fi-fe2025082787813
dc.language.isoen
dc.okm.affiliatedauthorFollain, Gautier
dc.okm.affiliatedauthorJacquemet, Guillaume
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNature Research
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41592-023-02057-w
dc.relation.ispartofjournalNature Methods
dc.source.identifierhttps://www.utupub.fi/handle/10024/190910
dc.titleHigh-fidelity 3D live-cell nanoscopy through data-driven enhanced super-resolution radial fluctuation
dc.year.issued2023

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