Cited 0 times in Scipus Cited Count

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

Authors
Song, KJ  | Song, KH | Na, BK | Kim, JH | Kwon, D  | Park, S  | Pak, JH | Im, KI | Shin, HJ
Citation
Parasitology research, 100(5). : 1083-1089, 2007
Journal Title
Parasitology research
ISSN
0932-01131432-1955
Abstract
A 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.
MeSH

DOI
10.1007/s00436-006-0404-8
PMID
17252278
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
Ajou Authors
권, 대호  |  박, 선  |  송, 경주  |  신, 호준
Files in This Item:
There are no files associated with this item.
Export

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

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

Browse