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Life and times: synthesis, trafficking, and evolution of VSG
Evasion of the acquired immune response in African trypanosomes is principally mediated by antigenic variation, the sequential expression of distinct variant surface glycoproteins (VSGs) at extremely high density on the cell surface. Sequence diversity between VSGs facilitates escape of a subpopulat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007029/ https://www.ncbi.nlm.nih.gov/pubmed/24731931 http://dx.doi.org/10.1016/j.pt.2014.03.004 |
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author | Manna, Paul T. Boehm, Cordula Leung, Ka Fai Natesan, Senthil Kumar Field, Mark C. |
author_facet | Manna, Paul T. Boehm, Cordula Leung, Ka Fai Natesan, Senthil Kumar Field, Mark C. |
author_sort | Manna, Paul T. |
collection | PubMed |
description | Evasion of the acquired immune response in African trypanosomes is principally mediated by antigenic variation, the sequential expression of distinct variant surface glycoproteins (VSGs) at extremely high density on the cell surface. Sequence diversity between VSGs facilitates escape of a subpopulation of trypanosomes from antibody-mediated killing. Significant advances have increased understanding of the mechanisms underpinning synthesis and maintenance of the VSG coat. In this review, we discuss the biosynthesis, trafficking, and turnover of VSG, emphasising those unusual mechanisms that act to maintain coat integrity and to protect against immunological attack. We also highlight new findings that suggest the presence of unique or highly divergent proteins that may offer therapeutic opportunities, as well as considering aspects of VSG biology that remain to be fully explored. |
format | Online Article Text |
id | pubmed-4007029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40070292014-05-05 Life and times: synthesis, trafficking, and evolution of VSG Manna, Paul T. Boehm, Cordula Leung, Ka Fai Natesan, Senthil Kumar Field, Mark C. Trends Parasitol Review Evasion of the acquired immune response in African trypanosomes is principally mediated by antigenic variation, the sequential expression of distinct variant surface glycoproteins (VSGs) at extremely high density on the cell surface. Sequence diversity between VSGs facilitates escape of a subpopulation of trypanosomes from antibody-mediated killing. Significant advances have increased understanding of the mechanisms underpinning synthesis and maintenance of the VSG coat. In this review, we discuss the biosynthesis, trafficking, and turnover of VSG, emphasising those unusual mechanisms that act to maintain coat integrity and to protect against immunological attack. We also highlight new findings that suggest the presence of unique or highly divergent proteins that may offer therapeutic opportunities, as well as considering aspects of VSG biology that remain to be fully explored. Elsevier Science 2014-05 /pmc/articles/PMC4007029/ /pubmed/24731931 http://dx.doi.org/10.1016/j.pt.2014.03.004 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Manna, Paul T. Boehm, Cordula Leung, Ka Fai Natesan, Senthil Kumar Field, Mark C. Life and times: synthesis, trafficking, and evolution of VSG |
title | Life and times: synthesis, trafficking, and evolution of VSG |
title_full | Life and times: synthesis, trafficking, and evolution of VSG |
title_fullStr | Life and times: synthesis, trafficking, and evolution of VSG |
title_full_unstemmed | Life and times: synthesis, trafficking, and evolution of VSG |
title_short | Life and times: synthesis, trafficking, and evolution of VSG |
title_sort | life and times: synthesis, trafficking, and evolution of vsg |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007029/ https://www.ncbi.nlm.nih.gov/pubmed/24731931 http://dx.doi.org/10.1016/j.pt.2014.03.004 |
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