Analysis of the stability of HLA-A2 molecules expressed on the cell surface

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dc.contributor.authorJong Seok Lim-
dc.contributor.authorKi Young Lee-
dc.contributor.authorHee Gu Lee-
dc.contributor.authorIk Hwan Kim-
dc.contributor.authorChong Kil Lee-
dc.contributor.authorSeong Sun Han-
dc.contributor.authorKil Hyoun Kim-
dc.date.accessioned2017-04-19T08:45:17Z-
dc.date.available2017-04-19T08:45:17Z-
dc.date.issued1996-
dc.identifier.issn1225-8687-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3696-
dc.description.abstractAssociation of antigenic peptide with class I MHC is believed to be crucial for maintaining stable conformation of class I molecules. T2 cells that are defective in TAP gene function mainly express class I molecules with an unstable conformation due to little or no association with antigenic peptides, whereas T1 cells that are normal in TAP gene function mainly express the stable form of class I molecules. In this work, attempts were made to determine the molecular stability of stable and unstable class I molecules. Dissociation of HLA-A2 molecules on T1 and T2 cells was monitored by flow cytomerry using anti-HLA-A2 antibody after the cells were treated with brefeldin A to shut down the transport of newly-assembled HLA-A2. Estimated dissociation rate constants for the stable and unstable forms of HLA-A2 were 0.076 h-1 and 0.66 h-1, respectively. It appeared that both T1 and T2 cells express stable and unstable class I complex, but with different ratios of the two forms. Furthermore, interferon-γ treatment of T1 cells appeared to induce the expression of both the stable and unstable class I molecules. These results demonstrate that class I MHC molecules can be divided into two groups in terms of structural stability and that they exist on the cell surface in both forms in a certain ratio.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleAnalysis of the stability of HLA-A2 molecules expressed on the cell surface-
dc.title.alternativeAnalysis of the stability of HLA-A2 molecules expressed on the cell surface-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number4-
dc.citation.endPage293-
dc.citation.startPage286-
dc.citation.volume29-
dc.contributor.affiliatedAuthorJong Seok Lim-
dc.contributor.affiliatedAuthorKi Young Lee-
dc.contributor.affiliatedAuthorHee Gu Lee-
dc.contributor.affiliatedAuthorIk Hwan Kim-
dc.contributor.alternativeName임종석-
dc.contributor.alternativeName이기영-
dc.contributor.alternativeName이희구-
dc.contributor.alternativeName김익환-
dc.contributor.alternativeName이종길-
dc.contributor.alternativeName한성순-
dc.contributor.alternativeName김길현-
dc.identifier.bibliographicCitationBMB Reports, vol. 29, no. 4, pp. 286-293-
dc.subject.keywordcell surface expression-
dc.subject.keyworddissociation rate constant-
dc.subject.keywordHLA-A2 molecule-
dc.subject.keywordinterferon-γ-
dc.subject.localcell surface expression-
dc.subject.localDissociation rate constant-
dc.subject.localdissociation rate constant-
dc.subject.localHLA-A2 Molecule-
dc.subject.localHLA-A2 molecule-
dc.subject.localInterferon gamma-
dc.subject.localInterferon γ-
dc.subject.localInterferon-γ-
dc.subject.localinterferon-gamma-
dc.subject.localinterferon-γ-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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