Full metadata record

DC Field Value Language
dc.contributor.authorHasan, Md Nabiul-
dc.contributor.authorPark, Soo Hyun-
dc.contributor.authorOh, Eulsik-
dc.contributor.authorSong, Eun Joo-
dc.contributor.authorBan, Eunmi-
dc.contributor.authorYoo, Young Sook-
dc.date.accessioned2024-01-20T18:03:39Z-
dc.date.available2024-01-20T18:03:39Z-
dc.date.created2021-09-05-
dc.date.issued2010-12-
dc.identifier.issn1615-9306-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130883-
dc.description.abstractAn analytical method of CE-MS and CE with an online preconcentration technique induced by a dynamic pH junction, addition of organic solvent and large volume injection was developed for sensitive determination of peptides in biological samples. Leucine enkephalin, methionine enkephalin, dynorphin A, beta-endorphin and angiotensin II were used as model peptides. The optimal online preconcentration conditions were obtained at a sample matrix consisting of 100 mM borate buffer (pH 10.0) with 50% v/v acetonitrile and a BGE containing 1 M formic acid at pH 2.0, along with a 25-cm injection length. Under the optimized conditions, a 4.0 x 10(3)-1.1 x 10(4)-fold increase in peak intensity was achieved without degrading the peak shape. This online preconcentration method was applied to analyze the intracellular angiotensin II within the peptides extracted from HL1 cells and approximately increase of 1 x 10(4)-fold sensitivity was achieved compared to normal condition. Thus, the developed method could be applied to the analysis of various peptides for peptidomics study in biological samples.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectRENIN-ANGIOTENSIN SYSTEM-
dc.subjectONLINE SAMPLE PRECONCENTRATION-
dc.subjectCAPILLARY-ELECTROPHORESIS-
dc.subjectMEDIATED STACKING-
dc.subjectPHYSIOLOGICAL SAMPLES-
dc.subjectLACTAM ANTIBIOTICS-
dc.subjectMASS-SPECTROMETRY-
dc.subjectHIGH-GLUCOSE-
dc.subjectTRANSIENT-
dc.subjectANIONS-
dc.titleSensitivity enhancement of CE and CE-MS for the analysis of peptides by a dynamic pH junction-
dc.typeArticle-
dc.identifier.doi10.1002/jssc.201000020-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF SEPARATION SCIENCE, v.33, no.23-24, pp.3701 - 3709-
dc.citation.titleJOURNAL OF SEPARATION SCIENCE-
dc.citation.volume33-
dc.citation.number23-24-
dc.citation.startPage3701-
dc.citation.endPage3709-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000285312700011-
dc.identifier.scopusid2-s2.0-78650149489-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusRENIN-ANGIOTENSIN SYSTEM-
dc.subject.keywordPlusONLINE SAMPLE PRECONCENTRATION-
dc.subject.keywordPlusCAPILLARY-ELECTROPHORESIS-
dc.subject.keywordPlusMEDIATED STACKING-
dc.subject.keywordPlusPHYSIOLOGICAL SAMPLES-
dc.subject.keywordPlusLACTAM ANTIBIOTICS-
dc.subject.keywordPlusMASS-SPECTROMETRY-
dc.subject.keywordPlusHIGH-GLUCOSE-
dc.subject.keywordPlusTRANSIENT-
dc.subject.keywordPlusANIONS-
dc.subject.keywordAuthorAngiotensin II-
dc.subject.keywordAuthorCE-
dc.subject.keywordAuthorCE-MS-
dc.subject.keywordAuthorDynamic pH junction-
dc.subject.keywordAuthorPeptide-
Appears in Collections:
KIST Article > 2010
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE