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dc.contributor.authorMålen, Hiwaen_US
dc.contributor.authorDe Souza, Gustavo A.en_US
dc.contributor.authorPathak, Sharaden_US
dc.contributor.authorSøfteland, Tinaen_US
dc.contributor.authorWiker, Harald G.en_US
dc.date.accessioned2012-01-23T15:18:22Z
dc.date.available2012-01-23T15:18:22Z
dc.date.issued2011-01-24eng
dc.PublishedBMC Microbiology 2011, 11:18en
dc.identifier.issn1471-2180
dc.identifier.urihttps://hdl.handle.net/1956/5508
dc.description.abstractBackground: The potential causes for variation in virulence between distinct M. tuberculosis strains are still not fully known. However, differences in protein expression are probably an important factor. In this study we used a labelfree quantitative proteomic approach to estimate differences in protein abundance between two closely related M. tuberculosis strains; the virulent H37Rv strain and its attenuated counterpart H37Ra. Results: We were able to identify more than 1700 proteins from both strains. As expected, the majority of the identified proteins had similar relative abundance in the two strains. However, 29 membrane-associated proteins were observed with a 5 or more fold difference in their relative abundance in one strain compared to the other. Of note, 19 membrane- and lipo-proteins had higher abundance in H37Rv, while another 10 proteins had a higher abundance in H37Ra. Interestingly, the possible protein-export membrane protein SecF (Rv2586c), and three ABCtransporter proteins (Rv0933, Rv1273c and Rv1819c) were among the more abundant proteins in M. tuberculosis H37Rv. Conclusion: Our data suggests that the bacterial secretion system and the transmembrane transport system may be important determinants of the ability of distinct M. tuberculosis strains to cause disease.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/eng
dc.titleComparison of membrane proteins of Mycobacterium tuberculosis H37Rv and H37Ra strainsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2011 Målen et al; licensee BioMed Central Ltd.
dc.identifier.doihttps://doi.org/10.1186/1471-2180-11-18
dc.identifier.cristin531516
dc.subject.nsiVDP::Mathematics and natural science: 400::Basic biosciences: 470::General microbiology: 472eng


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