dc.contributor.author |
Goolab, Shivani
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dc.contributor.author |
Roth, Robyn L
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dc.contributor.author |
Crampton, Michael C
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dc.contributor.author |
Van Heerden, H
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dc.date.accessioned |
2016-02-23T09:04:44Z |
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dc.date.available |
2016-02-23T09:04:44Z |
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dc.date.issued |
2015-10 |
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dc.identifier.citation |
Goolab, S., Roth, R.L., Crampton, M.C., and Van Heerden, H. Analyzing the molecular mechanism of lipoprotein localization in Brucella. Journal Frontiers in Microbiology, vol.6(1189), pp 20 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/10204/8408
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|
dc.description |
Copyright: 2015 Frontiers in Microbiology, vol. 6(1189),pp 20 |
en_US |
dc.description.abstract |
Bacterial lipoproteins possess diverse structure and functionality, ranging from bacterial physiology to pathogenic processes. As such many lipoproteins, originating from Brucella are exploited as potential vaccines to countermeasure brucellosis infection in the host. These membrane proteins are translocated from the cytoplasm to the cell membrane where they are anchored peripherally by a multifaceted targeting mechanism. Although much research has focused on the identification and classification of Brucellalipoproteins and their potential use as vaccine candidates for the treatment of Brucellosis, the underlying route for the translocation of these lipoproteins to the outer surface of the Brucella (and other pathogens) outer membrane (OM) remains mostly unknown. This is partly due to the complexity of the organism and evasive tactics used to escape the host immune system, the variation in biological structure and activity of lipoproteins, combined with the complex nature of the translocation machinery. The biosynthetic pathway ofBrucella lipoproteins involves a distinct secretion system aiding translocation from the cytoplasm, where they are modified by lipidation, sorted by the lipoprotein localization machinery pathway and thereafter equipped for export to the OM. Surface localized lipoproteins in Brucella may employ a lipoprotein flippase or the ß-barrel assembly complex for translocation. This review provides an overview of the characterized BrucellaOM proteins that form part of the OM, including a handful of other characterized bacterial lipoproteins and their mechanisms of translocation. Lipoprotein localization pathways in gram negative bacteria will be used as a model to identify gaps in Brucella lipoprotein localization and infer a potential pathway. Of particular interest are the dual topology lipoproteins identified in Escherichia coli and Haemophilus influenza. The localization and topology of these lipoproteins from other gram negative bacteria are well characterized and may be useful to infer a solution to better understand the translocation process in Brucella |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Frontiers Media |
en_US |
dc.relation.ispartofseries |
Workflow;15991 |
|
dc.subject |
Brucella vaccine target |
en_US |
dc.subject |
Lipoprotein localization |
en_US |
dc.subject |
Brucella lipoprotein |
en_US |
dc.subject |
Lipoprotein secretion |
en_US |
dc.subject |
Outer membrane protein |
en_US |
dc.subject |
Lol pathway |
en_US |
dc.subject |
Pathogen-associated molecular patterns |
en_US |
dc.subject |
Toll-like receptors |
en_US |
dc.title |
Analyzing the molecular mechanism of lipoprotein localization in Brucella |
en_US |
dc.type |
Article |
en_US |
dc.identifier.apacitation |
Goolab, S., Roth, R. L., Crampton, M. C., & Van Heerden, H. (2015). Analyzing the molecular mechanism of lipoprotein localization in Brucella. http://hdl.handle.net/10204/8408 |
en_ZA |
dc.identifier.chicagocitation |
Goolab, Shivani, Robyn L Roth, Michael C Crampton, and H Van Heerden "Analyzing the molecular mechanism of lipoprotein localization in Brucella." (2015) http://hdl.handle.net/10204/8408 |
en_ZA |
dc.identifier.vancouvercitation |
Goolab S, Roth RL, Crampton MC, Van Heerden H. Analyzing the molecular mechanism of lipoprotein localization in Brucella. 2015; http://hdl.handle.net/10204/8408. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Goolab, Shivani
AU - Roth, Robyn L
AU - Crampton, Michael C
AU - Van Heerden, H
AB - Bacterial lipoproteins possess diverse structure and functionality, ranging from bacterial physiology to pathogenic processes. As such many lipoproteins, originating from Brucella are exploited as potential vaccines to countermeasure brucellosis infection in the host. These membrane proteins are translocated from the cytoplasm to the cell membrane where they are anchored peripherally by a multifaceted targeting mechanism. Although much research has focused on the identification and classification of Brucellalipoproteins and their potential use as vaccine candidates for the treatment of Brucellosis, the underlying route for the translocation of these lipoproteins to the outer surface of the Brucella (and other pathogens) outer membrane (OM) remains mostly unknown. This is partly due to the complexity of the organism and evasive tactics used to escape the host immune system, the variation in biological structure and activity of lipoproteins, combined with the complex nature of the translocation machinery. The biosynthetic pathway ofBrucella lipoproteins involves a distinct secretion system aiding translocation from the cytoplasm, where they are modified by lipidation, sorted by the lipoprotein localization machinery pathway and thereafter equipped for export to the OM. Surface localized lipoproteins in Brucella may employ a lipoprotein flippase or the ß-barrel assembly complex for translocation. This review provides an overview of the characterized BrucellaOM proteins that form part of the OM, including a handful of other characterized bacterial lipoproteins and their mechanisms of translocation. Lipoprotein localization pathways in gram negative bacteria will be used as a model to identify gaps in Brucella lipoprotein localization and infer a potential pathway. Of particular interest are the dual topology lipoproteins identified in Escherichia coli and Haemophilus influenza. The localization and topology of these lipoproteins from other gram negative bacteria are well characterized and may be useful to infer a solution to better understand the translocation process in Brucella
DA - 2015-10
DB - ResearchSpace
DP - CSIR
KW - Brucella vaccine target
KW - Lipoprotein localization
KW - Brucella lipoprotein
KW - Lipoprotein secretion
KW - Outer membrane protein
KW - Lol pathway
KW - Pathogen-associated molecular patterns
KW - Toll-like receptors
LK - https://researchspace.csir.co.za
PY - 2015
T1 - Analyzing the molecular mechanism of lipoprotein localization in Brucella
TI - Analyzing the molecular mechanism of lipoprotein localization in Brucella
UR - http://hdl.handle.net/10204/8408
ER -
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en_ZA |