Cited 14 times in

Expression of tropomyosin from Blattella germanica as a recombinant non-fusion protein in Pichia pastoris and comparison of its IgE reactivity with its native counterpart

DC Field Value Language
dc.contributor.author용태순-
dc.contributor.author이한일-
dc.contributor.author정경용-
dc.date.accessioned2015-07-14T16:50:34Z-
dc.date.available2015-07-14T16:50:34Z-
dc.date.issued2004-
dc.identifier.issn1046-5928-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/111699-
dc.description.abstractTropomyosins derived from invertebrates are well-known pan allergens. However, the allergenicities of recombinant tropomyosins are variable. Here, we undertook to compare the IgE-binding reactivities of native and recombinant German cockroach tropomyosins. Native tropomyosin was purified by ammonium sulfate fractionation, hydroxyapatite column chromatography, and electroelution, and recombinant tropomyosin was expressed in Pichia pastoris. The allergenicities of the native and recombinant tropomyosins were compared by ELISA inhibition analysis. Native German cockroach tropomyosin showed 18% IgE-binding reactivity to German cockroach sensitized sera. Recombinant tropomyosin was produced without fusion protein and its N-terminus was blocked like that of the native counterpart. The IgE-binding reactivity of the recombinant was found to be comparable to that of native tropomyosin over the concentration range 1–1000 ng/ml by ELISA inhibition testing. Recombinant German cockroach tropomyosin expressed in Pichia pastoris showed better allergenicity than that expressed in Escherichia coli. Other factors in addition to the structural differences of native and recombinant proteins may also influence the IgE reactivities of tropomyosins.-
dc.description.statementOfResponsibilityopen-
dc.format.extent273~278-
dc.relation.isPartOfPROTEIN EXPRESSION AND PURIFICATION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleExpression of tropomyosin from Blattella germanica as a recombinant non-fusion protein in Pichia pastoris and comparison of its IgE reactivity with its native counterpart-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Environmental Medical Biology (환경의생물학)-
dc.contributor.googleauthorIn-Yong Lee-
dc.contributor.googleauthorKyoung Yong Jeong-
dc.contributor.googleauthorTai-Soon Yong-
dc.contributor.googleauthorHan-Il Ree-
dc.contributor.googleauthorChein-Soo Hong-
dc.contributor.googleauthorJongweon Lee-
dc.identifier.doi10.1016/j.pep.2004.06.009-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03572-
dc.relation.journalcodeJ02564-
dc.identifier.eissn1096-0279-
dc.identifier.pmid15358347-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S1046592804001962-
dc.contributor.alternativeNameYong, Tai Soon-
dc.contributor.alternativeNameRee, Han Il-
dc.rights.accessRightsnot free-
dc.citation.volume37-
dc.citation.number2-
dc.citation.startPage273-
dc.citation.endPage278-
dc.identifier.bibliographicCitationPROTEIN EXPRESSION AND PURIFICATION, Vol.37(2) : 273-278, 2004-
dc.identifier.rimsid37421-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Tropica Medicine (열대의학교실) > 1. Journal Papers

qrcode

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