DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, EY | - |
dc.contributor.author | Choi, DY | - |
dc.contributor.author | Kim, DK | - |
dc.contributor.author | Kim, JW | - |
dc.contributor.author | Park, JO | - |
dc.contributor.author | Kim, S | - |
dc.contributor.author | Kim, SH | - |
dc.contributor.author | Desiderio, DM | - |
dc.contributor.author | Kim, YK | - |
dc.contributor.author | Kim, KP | - |
dc.contributor.author | Gho, YS | - |
dc.date.accessioned | 2016-04-01T02:56:05Z | - |
dc.date.available | 2016-04-01T02:56:05Z | - |
dc.date.created | 2013-11-01 | - |
dc.date.issued | 2009-12 | - |
dc.identifier.issn | 1615-9853 | - |
dc.identifier.other | 2010-OAK-0000021108 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/26008 | - |
dc.description.abstract | Although archaea, Gram-negative bacteria, and mammalian cells constitutively secrete membrane vesicles (MVs) as a mechanism for cell-free intercellular communication, this cellular process has been overlooked in Gram-positive bacteria. Here, we found for the first time that Gram-positive bacteria naturally produce MVs into the extracellular milieu. Further characterizations showed that the density and size of Staphylococcus aureus-derived MVs are both similar to those of Gram-negative bacteria. With a proteomics approach, we identified with high confidence a total of 90 protein components of S. aureus-derived MVs. In the group of identified proteins, the highly enriched extracellular proteins suggested that a specific sorting mechanism for vesicular proteins exists. We also identified proteins that facilitate the transfer of proteins to other bacteria, as well to eliminate competing organisms, antibiotic resistance, pathological functions in systemic infections, and MV biogenesis. Taken together, these observations suggest that the secretion of MVs is an evolutionally conserved, universal process that occurs from simple organisms to complex multicellular organisms. This information will help us not only to elucidate the biogenesis and functions of MVs, but also to develop therapeutic tools for vaccines, diagnosis, and antibiotics effective against pathogenic strains of Gram-positive bacteria. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.relation.isPartOf | PROTEOMICS | - |
dc.subject | Gram-positive bacteria | - |
dc.subject | IgG-binding protein | - |
dc.subject | Membrane vesicles | - |
dc.subject | Microbiology | - |
dc.subject | Microvesicles | - |
dc.subject | Staphylococcus aureus | - |
dc.subject | ESCHERICHIA-COLI | - |
dc.subject | MASS-SPECTROMETRY | - |
dc.subject | PSEUDOMONAS-AERUGINOSA | - |
dc.subject | BACILLUS-SUBTILIS | - |
dc.subject | SEQUENCE-ANALYSIS | - |
dc.subject | PROTEIN | - |
dc.subject | CELL | - |
dc.subject | PATHOGENESIS | - |
dc.subject | STRATEGY | - |
dc.title | Gram-positive bacteria produce membrane vesicles: Proteomics-based characterization of Staphylococcus aureus-derived membrane vesicles | - |
dc.type | Article | - |
dc.contributor.college | 생명과학과 | - |
dc.identifier.doi | 10.1002/PMIC.200900338 | - |
dc.author.google | Lee, EY | - |
dc.author.google | Choi, DY | - |
dc.author.google | Kim, DK | - |
dc.author.google | Kim, JW | - |
dc.author.google | Park, JO | - |
dc.author.google | Kim, S | - |
dc.author.google | Kim, SH | - |
dc.author.google | Desiderio, DM | - |
dc.author.google | Kim, YK | - |
dc.author.google | Kim, KP | - |
dc.author.google | Gho, YS | - |
dc.relation.volume | 9 | - |
dc.relation.issue | 24 | - |
dc.relation.startpage | 5425 | - |
dc.relation.lastpage | 5436 | - |
dc.contributor.id | 10138843 | - |
dc.relation.journal | PROTEOMICS | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | PROTEOMICS, v.9, no.24, pp.5425 - 5436 | - |
dc.identifier.wosid | 000273515000005 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 5436 | - |
dc.citation.number | 24 | - |
dc.citation.startPage | 5425 | - |
dc.citation.title | PROTEOMICS | - |
dc.citation.volume | 9 | - |
dc.contributor.affiliatedAuthor | Gho, YS | - |
dc.identifier.scopusid | 2-s2.0-73149088617 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 180 | - |
dc.description.scptc | 162 | * |
dc.date.scptcdate | 2018-05-121 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | ESCHERICHIA-COLI | - |
dc.subject.keywordPlus | MASS-SPECTROMETRY | - |
dc.subject.keywordPlus | PSEUDOMONAS-AERUGINOSA | - |
dc.subject.keywordPlus | BACILLUS-SUBTILIS | - |
dc.subject.keywordPlus | SEQUENCE-ANALYSIS | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordPlus | CELL | - |
dc.subject.keywordPlus | PATHOGENESIS | - |
dc.subject.keywordPlus | STRATEGY | - |
dc.subject.keywordAuthor | Gram-positive bacteria | - |
dc.subject.keywordAuthor | IgG-binding protein | - |
dc.subject.keywordAuthor | Membrane vesicles | - |
dc.subject.keywordAuthor | Microbiology | - |
dc.subject.keywordAuthor | Microvesicles | - |
dc.subject.keywordAuthor | Staphylococcus aureus | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
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