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Allergenic characterization of tropomyosin from the dusky brown cockroach, Periplaneta fuliginosa

DC Field Value Language
dc.contributor.author이인용-
dc.contributor.author이종원-
dc.contributor.author이한일-
dc.contributor.author정경용-
dc.contributor.author홍천수-
dc.contributor.author김동수-
dc.contributor.author용태순-
dc.date.accessioned2015-07-14T17:26:10Z-
dc.date.available2015-07-14T17:26:10Z-
dc.date.issued2004-
dc.identifier.issn1071-412X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/112877-
dc.description.abstractHousehold arthropods are one of the most common causes of allergic diseases. Four species of cockroaches are found to reside in Korean homes, but published work deals almost exclusively with the German and American cockroaches. This study was undertaken to investigate the cross-reactive allergenic components of the dusky brown cockroach, Periplaneta fuliginosa. Enzyme-linked immunosorbent assay (ELISA) inhibition and immunoblot analyses for the dusky brown cockroach were performed with Blattella germanica and Dermatophagoides farinae allergic sera. cDNA encoding tropomyosin, which is a well known cross-reactive pan-allergen, was cloned by reverse transcriptase PCR, and recombinant protein was produced by using a pET-28b expression system. Native tropomyosin was purified by ammonium sulfate fractionation and electroelution. The immunoglobulin E (IgE) reactivities of native and recombinant tropomyosins were compared by an ELISA inhibition study. All 30 sera tested showed P. fuliginosa-specific IgE, and the IgE-binding reactivity of the P. fuliginosa extract was inhibited as much as 79.4% by a B. germanica extract and as much as 63.3% by a D. farinae extract. The deduced amino acid sequence of cloned cDNA was identical with that of Periplaneta americana tropomyosin (98.5% nucleotide sequence identity). Seven of 26 (26.9%) allergic sera had IgE specific for recombinant protein, and the maximum inhibition of P. fuliginosa-specific IgE achieved with recombinant tropomyosin was 37.7% at an inhibitor concentration of 10 μg/ml. Native tropomyosin inhibited the binding of IgE to the P. fuliginosa, B. germanica, and D. farinae extracts by 65.0, 51.8, and 39% at an inhibitor concentration of 1 μg/ml. P. fuliginosa appears to possess allergens that are highly cross-reactive with allergens of B. germanica and D. farinae. Tropomyosin was found to be a major allergenic component accounting for the cross-reactivity between cockroaches and dust mites.-
dc.description.statementOfResponsibilityopen-
dc.format.extent680~685-
dc.relation.isPartOfCLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHAmino Acid Sequence-
dc.subject.MESHAnimals-
dc.subject.MESHBase Sequence-
dc.subject.MESHChild-
dc.subject.MESHCloning, Molecular-
dc.subject.MESHCross Reactions-
dc.subject.MESHDNA, Complementary/analysis-
dc.subject.MESHElectrophoresis, Polyacrylamide Gel-
dc.subject.MESHEnzyme-Linked Immunosorbent Assay-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHImmunoblotting-
dc.subject.MESHImmunoglobulin E/immunology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMolecular Sequence Data-
dc.subject.MESHPeriplaneta/genetics-
dc.subject.MESHPeriplaneta/immunology*-
dc.subject.MESHRecombinant Proteins/genetics-
dc.subject.MESHRecombinant Proteins/immunology*-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHSequence Homology-
dc.subject.MESHSpecies Specificity-
dc.subject.MESHTropomyosin/genetics*-
dc.subject.MESHTropomyosin/immunology*-
dc.titleAllergenic characterization of tropomyosin from the dusky brown cockroach, Periplaneta fuliginosa-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorKyoung Yong Jeong-
dc.contributor.googleauthorHeeyu Hwang-
dc.contributor.googleauthorTai-Soon Yong-
dc.contributor.googleauthorHan-Il Ree-
dc.contributor.googleauthorChein-Soo Hong-
dc.contributor.googleauthorDong Soo Kim-
dc.contributor.googleauthorIn-Yong Lee-
dc.contributor.googleauthorJongweon Lee-
dc.identifier.doi10.1128/CDLI.11.4.680-685.2004-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03059-
dc.contributor.localIdA03144-
dc.contributor.localIdA03279-
dc.contributor.localIdA03572-
dc.contributor.localIdA02424-
dc.contributor.localIdA00405-
dc.contributor.localIdA04448-1-
dc.relation.journalcodeJ00547-
dc.identifier.eissn1098-6588-
dc.identifier.pmid15242941-
dc.contributor.alternativeNameLee, In Yong-
dc.contributor.alternativeNameLee, Jong Weon-
dc.contributor.alternativeNameRee, Han Il-
dc.contributor.alternativeNameJeong, Kyoung Yong-
dc.contributor.alternativeNameHong, Chein Soo-
dc.contributor.alternativeNameKim, Dong Soo-
dc.contributor.alternativeNameYong, Tai Soon-
dc.contributor.affiliatedAuthorLee, In Yong-
dc.contributor.affiliatedAuthorLee, Jong Weon-
dc.contributor.affiliatedAuthorRee, Han Il-
dc.contributor.affiliatedAuthorJeong, Kyoung Yong-
dc.contributor.affiliatedAuthorYong, Tai Soon-
dc.contributor.affiliatedAuthorKim, Dong Soo-
dc.contributor.affiliatedAuthorHong, Chein Soo-
dc.rights.accessRightsfree-
dc.citation.volume11-
dc.citation.number4-
dc.citation.startPage680-
dc.citation.endPage685-
dc.identifier.bibliographicCitationCLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY , Vol.11(4) : 680-685, 2004-
dc.identifier.rimsid36770-
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
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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