Cited 0 times in Scipus Cited Count

Molecular cloning and characterization of a cytosolic heat shock protein 70 from Naegleria fowleri.

DC Field Value Language
dc.contributor.authorSong, KJ-
dc.contributor.authorSong, KH-
dc.contributor.authorNa, BK-
dc.contributor.authorKim, JH-
dc.contributor.authorKwon, D-
dc.contributor.authorPark, S-
dc.contributor.authorPak, JH-
dc.contributor.authorIm, KI-
dc.contributor.authorShin, HJ-
dc.date.accessioned2011-01-19T05:03:44Z-
dc.date.available2011-01-19T05:03:44Z-
dc.date.issued2007-
dc.identifier.issn0932-0113-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/1218-
dc.description.abstractA gene encoding a cytosolic heat shock protein 70 from pathogenic Naegleria fowleri (Nf-cHSP70) was identified. The Nf-cHSP70 was 2,062 bp in length with an open reading frame of 1,980 bp encoding 659 amino acid residues. The deduced amino acid sequence of the gene shared high sequence identities with HSP70s from other parasitic organisms and mammals. The characteristic domains, including N-terminal ATPase domain, calmodulin-binding domain, and EE(D)VD motif, found in HSP70s were also well conserved in this gene. The recombinant Nf-cHSP70 protein showed strong antigenicity against the sera from mice experimentally infected with N. fowleri. Immunofluorescence assay showed that Nf-cHSP70 localized in cytosol of the parasite. The results from semi-quantitative RT-PCR and Western blot analyses demonstrated the expression levels of gene transcripts, and its products were significantly increased at high temperature (42 degrees C). The definitive biological roles of Nf-cHSP70 are not clear, but it may protect the parasite under environmental changes especially high temperature.-
dc.language.isoen-
dc.subject.MESHAmino Acid Motifs-
dc.subject.MESHAmino Acid Sequence-
dc.subject.MESHAnimals-
dc.subject.MESHCloning, Molecular-
dc.subject.MESHConserved Sequence-
dc.subject.MESHCytosol-
dc.subject.MESHDNA, Protozoan-
dc.subject.MESHGene Expression Regulation-
dc.subject.MESHHSP70 Heat-Shock Proteins-
dc.subject.MESHMicroscopy, Fluorescence-
dc.subject.MESHMolecular Sequence Data-
dc.subject.MESHNaegleria fowleri-
dc.subject.MESHOpen Reading Frames-
dc.subject.MESHProtein Structure, Tertiary-
dc.subject.MESHProtozoan Proteins-
dc.subject.MESHRNA, Messenger-
dc.subject.MESHRNA, Protozoan-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHSequence Analysis, DNA-
dc.subject.MESHSequence Homology, Amino Acid-
dc.subject.MESHTemperature-
dc.titleMolecular cloning and characterization of a cytosolic heat shock protein 70 from Naegleria fowleri.-
dc.typeArticle-
dc.identifier.pmid17252278-
dc.contributor.affiliatedAuthor송, 경주-
dc.contributor.affiliatedAuthor권, 대호-
dc.contributor.affiliatedAuthor박, 선-
dc.contributor.affiliatedAuthor신, 호준-
dc.type.localJournal Papers-
dc.identifier.doi10.1007/s00436-006-0404-8-
dc.citation.titleParasitology research-
dc.citation.volume100-
dc.citation.number5-
dc.citation.date2007-
dc.citation.startPage1083-
dc.citation.endPage1089-
dc.identifier.bibliographicCitationParasitology research, 100(5). : 1083-1089, 2007-
dc.identifier.eissn1432-1955-
dc.relation.journalidJ009320113-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
Files in This Item:
There are no files associated with this item.

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

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

Browse