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Analyzing the molecular mechanism of lipoprotein localization in Brucella

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 tra...

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Autores principales: Goolab, Shivani, Roth, Robyn L., van Heerden, Henriette, Crampton, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623201/
https://www.ncbi.nlm.nih.gov/pubmed/26579096
http://dx.doi.org/10.3389/fmicb.2015.01189
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author Goolab, Shivani
Roth, Robyn L.
van Heerden, Henriette
Crampton, Michael C.
author_facet Goolab, Shivani
Roth, Robyn L.
van Heerden, Henriette
Crampton, Michael C.
author_sort Goolab, Shivani
collection PubMed
description 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 Brucella lipoproteins 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 of Brucella 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 β-barrel assembly complex for translocation. This review provides an overview of the characterized Brucella OM 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.
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spelling pubmed-46232012015-11-17 Analyzing the molecular mechanism of lipoprotein localization in Brucella Goolab, Shivani Roth, Robyn L. van Heerden, Henriette Crampton, Michael C. Front Microbiol Microbiology 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 Brucella lipoproteins 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 of Brucella 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 β-barrel assembly complex for translocation. This review provides an overview of the characterized Brucella OM 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. Frontiers Media S.A. 2015-10-28 /pmc/articles/PMC4623201/ /pubmed/26579096 http://dx.doi.org/10.3389/fmicb.2015.01189 Text en Copyright © 2015 Goolab, Roth, van Heerden and Crampton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Goolab, Shivani
Roth, Robyn L.
van Heerden, Henriette
Crampton, Michael C.
Analyzing the molecular mechanism of lipoprotein localization in Brucella
title Analyzing the molecular mechanism of lipoprotein localization in Brucella
title_full Analyzing the molecular mechanism of lipoprotein localization in Brucella
title_fullStr Analyzing the molecular mechanism of lipoprotein localization in Brucella
title_full_unstemmed Analyzing the molecular mechanism of lipoprotein localization in Brucella
title_short Analyzing the molecular mechanism of lipoprotein localization in Brucella
title_sort analyzing the molecular mechanism of lipoprotein localization in brucella
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623201/
https://www.ncbi.nlm.nih.gov/pubmed/26579096
http://dx.doi.org/10.3389/fmicb.2015.01189
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