Photoexcited Porphyrins as a Strong Suppressor of beta-Amyloid Aggregation and Synaptic Toxicity

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dc.contributor.authorLee, Byung Ilko
dc.contributor.authorLee, Seongsooko
dc.contributor.authorSuh, Yoon Seokko
dc.contributor.authorLee, Joon Seokko
dc.contributor.authorKim, Ae-kyeongko
dc.contributor.authorKwon, O-Yuko
dc.contributor.authorYu, Kweonko
dc.contributor.authorPark, Chan Beumko
dc.date.accessioned2016-04-20T06:25:26Z-
dc.date.available2016-04-20T06:25:26Z-
dc.date.created2015-11-30-
dc.date.created2015-11-30-
dc.date.issued2015-09-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.54, no.39, pp.11472 - 11476-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/205325-
dc.description.abstractThe abnormal assembly of beta-amyloid (Ab) peptides into neurotoxic, beta-sheet-rich amyloid aggregates is a major pathological hallmark of Alzheimer's disease (AD). Light-induced photosensitizing molecules can regulate A beta amyloidogenesis. Multiple photochemical analyses using circular dichroism, atomic force microscopy, dot blot, and native gel electrophoresis verified that photoactivated meso-tetra(4-sulfonatophenyl)porphyrin (TPPS with M = 2H(+), Zn2+, Cu2+, Mn2+) successfully inhibits A beta aggregation in vitro. Furthermore, A beta toxicity was relieved in the photoexcited-TPP-Streated Drosophila AD model. TPPS suppresses neural cell death, synaptic toxicity, and behavioral defects in the Drosophila AD model under blue light illumination. Behavioral phenotypes, including larval locomotion defect and short lifespan caused by A beta overexpression, were also rescued by blue light-excited TPPS.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectTAU AGGREGATION-
dc.subjectDROSOPHILA-
dc.subjectPROTEIN-
dc.subjectPEPTIDE-
dc.subjectMODELS-
dc.subjectINHIBITION-
dc.subjectCOMPLEXES-
dc.subjectWATER-
dc.titlePhotoexcited Porphyrins as a Strong Suppressor of beta-Amyloid Aggregation and Synaptic Toxicity-
dc.typeArticle-
dc.identifier.wosid000363392100020-
dc.identifier.scopusid2-s2.0-84942163156-
dc.type.rimsART-
dc.citation.volume54-
dc.citation.issue39-
dc.citation.beginningpage11472-
dc.citation.endingpage11476-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.201504310-
dc.contributor.localauthorPark, Chan Beum-
dc.contributor.nonIdAuthorLee, Seongsoo-
dc.contributor.nonIdAuthorSuh, Yoon Seok-
dc.contributor.nonIdAuthorKim, Ae-kyeong-
dc.contributor.nonIdAuthorKwon, O-Yu-
dc.contributor.nonIdAuthorYu, Kweon-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorDrosophila model-
dc.subject.keywordAuthorphotosensitizers-
dc.subject.keywordAuthorporphyrins-
dc.subject.keywordAuthorbeta-amyloids-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusTAU AGGREGATION-
dc.subject.keywordPlusDROSOPHILA-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusMODELS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusWATER-
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