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Influence of Aromatic Residues on the Material Characteristics of A Amyloid Protofibrils at the Atomic Scale

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dc.contributor.authorChang, Hyun Joon-
dc.contributor.authorBaek, Inchul-
dc.contributor.authorLee, Myeongsang-
dc.contributor.authorNa, Sungsoo-
dc.date.accessioned2021-09-04T13:33:44Z-
dc.date.available2021-09-04T13:33:44Z-
dc.date.created2021-06-18-
dc.date.issued2015-08-03-
dc.identifier.issn1439-4235-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/92780-
dc.description.abstractAmyloid fibrils, which cause a number of degenerative diseases, are insoluble under physiological conditions and are supported by native contacts. Recently, the effects of the aromatic residues on the A amyloid protofibril were investigated in a ThT fluorescence study. However, the relationship between the material characteristics of the A protofibril and its aromatic residues has not yet been investigated on the atomic scale. Here, we successfully constructed wild-type (WT) and mutated types of A protofibrils by using molecular dynamics simulations. Through principle component analysis, we established the structural stability and vibrational characteristics of F20L A protofibrils and compared them with WT and other mutated models such as F19L and F19LF20L. In addition, structural stability was assessed by calculating the elastic modulus, which showed that the F20L model has higher values than the other models studied. From our results, it is shown that aromatic residues influence the structural and material characteristics of A protofibrils.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectMOLECULAR-DYNAMICS SIMULATIONS-
dc.subjectNORMAL-MODE ANALYSIS-
dc.subjectFORCE MICROSCOPY-
dc.subjectTECHNOLOGICAL APPLICATIONS-
dc.subjectMECHANICAL-PROPERTIES-
dc.subjectPHYSICAL-PROPERTIES-
dc.subjectBETA-PEPTIDE-
dc.subjectFIBRILS-
dc.subjectPROTEIN-
dc.subjectAGGREGATION-
dc.titleInfluence of Aromatic Residues on the Material Characteristics of A Amyloid Protofibrils at the Atomic Scale-
dc.typeArticle-
dc.contributor.affiliatedAuthorNa, Sungsoo-
dc.identifier.doi10.1002/cphc.201500244-
dc.identifier.scopusid2-s2.0-84937969810-
dc.identifier.wosid000358538300018-
dc.identifier.bibliographicCitationCHEMPHYSCHEM, v.16, no.11, pp.2403 - 2414-
dc.relation.isPartOfCHEMPHYSCHEM-
dc.citation.titleCHEMPHYSCHEM-
dc.citation.volume16-
dc.citation.number11-
dc.citation.startPage2403-
dc.citation.endPage2414-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.subject.keywordPlusMOLECULAR-DYNAMICS SIMULATIONS-
dc.subject.keywordPlusNORMAL-MODE ANALYSIS-
dc.subject.keywordPlusFORCE MICROSCOPY-
dc.subject.keywordPlusTECHNOLOGICAL APPLICATIONS-
dc.subject.keywordPlusMECHANICAL-PROPERTIES-
dc.subject.keywordPlusPHYSICAL-PROPERTIES-
dc.subject.keywordPlusBETA-PEPTIDE-
dc.subject.keywordPlusFIBRILS-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusAGGREGATION-
dc.subject.keywordAuthoramyloid beta-peptides-
dc.subject.keywordAuthormechanical properties-
dc.subject.keywordAuthormolecular dynamics-
dc.subject.keywordAuthormolecular modeling-
dc.subject.keywordAuthorstacking interactions-
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