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분자분광학및동력학연구단
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Label-free adaptive optics single-molecule localization microscopy for whole zebrafish

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dc.contributor.authorSanghyeon Park-
dc.contributor.authorYonghyeon Jo-
dc.contributor.authorKang, Minsu-
dc.contributor.authorJin Hee Hong-
dc.contributor.authorKo, Sangyoon-
dc.contributor.authorKim, Suhyun-
dc.contributor.authorPark, Sangjun-
dc.contributor.authorPark, Hae Chul-
dc.contributor.authorShim, Sang-Hee-
dc.contributor.authorWonshik Choi-
dc.date.accessioned2023-09-15T22:00:50Z-
dc.date.available2023-09-15T22:00:50Z-
dc.date.created2023-07-24-
dc.date.issued2023-07-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/13938-
dc.description.abstractSpecimen-induced aberration has been a major factor limiting the imaging depth of single-molecule localization microscopy (SMLM). Here, we report the application of label-free wavefront sensing adaptive optics to SMLM for deep-tissue super-resolution imaging. The proposed system measures complex tissue aberrations from intrinsic reflectance rather than fluorescence emission and physically corrects the wavefront distortion more than three-fold stronger than the previous limit. This enables us to resolve sub-diffraction morphologies of cilia and oligodendrocytes in whole zebrafish as well as dendritic spines in thick mouse brain tissues at the depth of up to 102 μm with localization number enhancement by up to 37 times and localization precision comparable to aberration-free samples. The proposed approach can expand the application range of SMLM to whole zebrafish that cause the loss of localization number owing to severe tissue aberrations. © 2023. The Author(s).-
dc.language영어-
dc.publisherNLM (Medline)-
dc.titleLabel-free adaptive optics single-molecule localization microscopy for whole zebrafish-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid001030405300026-
dc.identifier.scopusid2-s2.0-85164846859-
dc.identifier.rimsid81241-
dc.contributor.affiliatedAuthorSanghyeon Park-
dc.contributor.affiliatedAuthorYonghyeon Jo-
dc.contributor.affiliatedAuthorJin Hee Hong-
dc.contributor.affiliatedAuthorWonshik Choi-
dc.identifier.doi10.1038/s41467-023-39896-2-
dc.identifier.bibliographicCitationNature communications, v.14, no.1-
dc.relation.isPartOfNature communications-
dc.citation.titleNature communications-
dc.citation.volume14-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusSTED MICROSCOPY-
dc.subject.keywordPlusNERVOUS-SYSTEM-
dc.subject.keywordPlusSUPERRESOLUTION-
dc.subject.keywordPlusOLIGODENDROCYTES-
dc.subject.keywordPlusABERRATIONS-
dc.subject.keywordPlusMYELIN-
dc.subject.keywordPlusCELLS-
Appears in Collections:
Center for Molecular Spectroscopy and Dynamics(분자 분광학 및 동력학 연구단) > 1. Journal Papers (저널논문)
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