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dc.contributor.author김두리-
dc.date.accessioned2019-11-19T05:40:16Z-
dc.date.available2019-11-19T05:40:16Z-
dc.date.issued2017-01-
dc.identifier.citationCHEMICAL REVIEWS, v. 117, no. 11, page. 7428-7456en_US
dc.identifier.issn0009-2665-
dc.identifier.issn1520-6890-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.chemrev.6b00604-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/112312-
dc.description.abstractCorrelative microscopy, the integration of two or more microscopy techniques performed on the same sample, produces results that emphasize the strengths of each technique while offsetting their individual weaknesses. Light microscopy has historically been a central method in correlative microscopy due to its widespread availability, compatibility with hydrated and live biological samples, and excellent molecular specificity through fluorescence labeling. However, conventional light microscopy can only achieve a resolution of similar to 300 nm, undercutting its advantages in correlations with higher-resolution methods. The rise of super-resolution microscopy (SRM) over the past decade has drastically improved the resolution of light microscopy to similar to 10 nm, thus creating exciting new opportunities and challenges for correlative microscopy. Here we review how these challenges are addressed to effectively correlate SRM with other microscopy techniques, including light microscopy, electron microscopy, cryomicroscopy, atomic force microscopy, and various forms of spectroscopy. Though we emphasize biological studies, we also discuss the application of correlative SRM to materials characterization and single-molecule reactions. Finally, we point out current limitations and discuss possible future improvements and advances. We thus demonstrate how a correlative approach adds new dimensions of information and provides new opportunities in the fast-growing field of SRM.en_US
dc.description.sponsorshipWe thank Professor Stephen Leone for helpful comments. We acknowledge support from the National Science Foundation under CHE-1554717, the Pew Biomedical Scholars Award, the Beckman Young Investigator Program, the Sloan Research Fellowship, the Hellman Fellows Fund, the Bakar Fellows Award, the Department of Chemistry at UC Berkeley, and the LDRD Program of LBNL under DOE (DE-AC02-05CH11231). M.W. acknowledges support from the NSF Graduate Research Fellowship under DGE 1106400.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectATOMIC-FORCE MICROSCOPYen_US
dc.subjectPHOTOACTIVATABLE FLUORESCENT PROTEINSen_US
dc.subjectMOLECULE LOCALIZATION MICROSCOPYen_US
dc.subjectLIGHT-ELECTRON MICROSCOPYen_US
dc.subjectION MASS-SPECTROMETRYen_US
dc.subjectHIGH-SPEED AFMen_US
dc.subjectSINGLE-MOLECULEen_US
dc.subjectLIVE-CELLen_US
dc.subjectLIVING CELLSen_US
dc.subjectCRYOELECTRON TOMOGRAPHYen_US
dc.titleCorrelative Super-Resolution Microscopy: New Dimensions and New Opportunitiesen_US
dc.typeArticleen_US
dc.relation.no11-
dc.relation.volume117-
dc.identifier.doi10.1021/acs.chemrev.6b00604-
dc.relation.page7428-7456-
dc.relation.journalCHEMICAL REVIEWS-
dc.contributor.googleauthorHauser, Meghan-
dc.contributor.googleauthorWojcik, Michal-
dc.contributor.googleauthorKim, Doory-
dc.contributor.googleauthorMahmoudi, Morteza-
dc.contributor.googleauthorLi, Wan-
dc.contributor.googleauthorXu, Ke-
dc.relation.code2017000252-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.piddoorykim-
Appears in Collections:
COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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