DC Field | Value | Language |
---|---|---|
dc.contributor.author | Go, MY | - |
dc.contributor.author | Kim, S | - |
dc.contributor.author | Partridge, AW | - |
dc.contributor.author | Melnyk, RA | - |
dc.contributor.author | Rath, A | - |
dc.contributor.author | Deber, CM | - |
dc.contributor.author | Mogridge, J | - |
dc.date.accessioned | 2016-04-01T01:53:23Z | - |
dc.date.available | 2016-04-01T01:53:23Z | - |
dc.date.created | 2009-02-28 | - |
dc.date.issued | 2006-06-30 | - |
dc.identifier.issn | 0022-2836 | - |
dc.identifier.other | 2006-OAK-0000006061 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/23932 | - |
dc.description.abstract | Protective antigen (PA), lethal factor (LF) and edema factor (EF) are secreted individually by Bacillus anthracis. These components of anthrax toxin must then assemble into complexes to intoxicate mammalian cells. Toxin assembly it-vitiates when molecules of PA bind mammalian receptors ANTXR1/2 and are cleaved by surface proteases into 20 kDa and 63 kDa fragments. After PA(20) dissociates, receptor-bound PA(63) homo-oligomerizes into heptamers. Oligomeric PA(63) binds EF and LF and these complexes are internalized into an acidic compartment where the two enzymatic components are translocated across the membrane by a channel formed by heptameric PA(63). Since oligomerization of PA(63) is required to bind and translocate the enzymatic components, we sought to determine whether interactions between toxin receptors could facilitate the assembly process. In the present work, we performed a co-immunoprecipitation experiment to demonstrate that ANTXR1 is oligomeric in mammalian cells. Computer modeling predicted the self-association of the ANTXR1 transmembrane domain and we detected oligomerization of ANTXR1 transmembrane domain peptides in the membrane-mimetic environment of SDS micelles using fluorescence resonance energy transfer. Furthermore, the ANTXR1 transmembrane domain mediated oligomerization of a reporter protein construct in a bacterial membrane. In both assays, mutations that disrupted the interaction were consistent with the interaction being mediated through an asymmetric binding interface. Mutations that impaired self-association of the transmembrane domain reduced the rate of PA(63) heptamer formation on the mammalian cell surface. Our findings indicate that ANTXR1 transmembrane domains self-associate and that these interactions may stabilize intermediate oligomerization states of ANTXR1-PA(63) complexes. (c) 2006 Elsevier Ltd. All rights reserved. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | ACADEMIC PRESS LTD ELSEVIER SCIENCE L | - |
dc.relation.isPartOf | JOURNAL OF MOLECULAR BIOLOGY | - |
dc.subject | anthrax | - |
dc.subject | ANTXR1 | - |
dc.subject | transmembrane | - |
dc.subject | fluorescence resonance energy transfer | - |
dc.subject | TOXCAT | - |
dc.subject | CAPILLARY MORPHOGENESIS PROTEIN-2 | - |
dc.subject | SPANNING LEUCINE-ZIPPER | - |
dc.subject | PROTECTIVE ANTIGEN | - |
dc.subject | ERYTHROPOIETIN RECEPTOR | - |
dc.subject | HELIX ASSOCIATION | - |
dc.subject | CRYSTAL-STRUCTURE | - |
dc.subject | LETHAL FACTOR | - |
dc.subject | GXXXG MOTIFS | - |
dc.subject | MEMBRANE | - |
dc.subject | PORE | - |
dc.title | Self-association of the transmembrane domain of an anthrax toxin receptor | - |
dc.type | Article | - |
dc.contributor.college | 생명과학과 | - |
dc.identifier.doi | 10.1016/j.jmb.2006.04.072 | - |
dc.author.google | Go, MY | - |
dc.author.google | Kim, S | - |
dc.author.google | Partridge, AW | - |
dc.author.google | Melnyk, RA | - |
dc.author.google | Rath, A | - |
dc.author.google | Deber, CM | - |
dc.author.google | Mogridge, J | - |
dc.relation.volume | 360 | - |
dc.relation.issue | 1 | - |
dc.relation.startpage | 145 | - |
dc.relation.lastpage | 156 | - |
dc.contributor.id | 10136479 | - |
dc.relation.journal | JOURNAL OF MOLECULAR BIOLOGY | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | JOURNAL OF MOLECULAR BIOLOGY, v.360, no.1, pp.145 - 156 | - |
dc.identifier.wosid | 000238844500014 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 156 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 145 | - |
dc.citation.title | JOURNAL OF MOLECULAR BIOLOGY | - |
dc.citation.volume | 360 | - |
dc.contributor.affiliatedAuthor | Kim, S | - |
dc.identifier.scopusid | 2-s2.0-33745459428 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 20 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | CAPILLARY MORPHOGENESIS PROTEIN-2 | - |
dc.subject.keywordPlus | PROTECTIVE ANTIGEN | - |
dc.subject.keywordPlus | CRYSTAL-STRUCTURE | - |
dc.subject.keywordPlus | LETHAL FACTOR | - |
dc.subject.keywordPlus | GXXXG MOTIFS | - |
dc.subject.keywordPlus | STOICHIOMETRY | - |
dc.subject.keywordPlus | TRANSLOCATION | - |
dc.subject.keywordPlus | STABILIZES | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | PREDICTION | - |
dc.subject.keywordAuthor | anthrax | - |
dc.subject.keywordAuthor | ANTXR1 | - |
dc.subject.keywordAuthor | transmembrane | - |
dc.subject.keywordAuthor | fluorescence resonance energy transfer | - |
dc.subject.keywordAuthor | TOXCAT | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
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