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Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family

Trans-sialidases are key enzymes in the life cycle of African trypanosomes in both, mammalian host and insect vector and have been associated with the disease trypanosomiasis, namely sleeping sickness and nagana. Besides the previously reported TconTS1, we have identified three additional active tra...

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Autores principales: Gbem, Thaddeus T., Waespy, Mario, Hesse, Bettina, Dietz, Frank, Smith, Joel, Chechet, Gloria D., Nok, Jonathan A., Kelm, Sørge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855035/
https://www.ncbi.nlm.nih.gov/pubmed/24340108
http://dx.doi.org/10.1371/journal.pntd.0002549
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author Gbem, Thaddeus T.
Waespy, Mario
Hesse, Bettina
Dietz, Frank
Smith, Joel
Chechet, Gloria D.
Nok, Jonathan A.
Kelm, Sørge
author_facet Gbem, Thaddeus T.
Waespy, Mario
Hesse, Bettina
Dietz, Frank
Smith, Joel
Chechet, Gloria D.
Nok, Jonathan A.
Kelm, Sørge
author_sort Gbem, Thaddeus T.
collection PubMed
description Trans-sialidases are key enzymes in the life cycle of African trypanosomes in both, mammalian host and insect vector and have been associated with the disease trypanosomiasis, namely sleeping sickness and nagana. Besides the previously reported TconTS1, we have identified three additional active trans-sialidases, TconTS2, TconTS3 and TconTS4, and three trans-sialidase like genes in Trypanosoma congolense. At least TconTS1, TconTS2 and TconTS4 are found in the bloodstream of infected animals. We have characterised the enzymatic properties of recombinant proteins expressed in eukaryotic fibroblasts using fetuin as model blood glycoprotein donor substrate. One of the recombinant trans-sialidases, TconTS2, had the highest specific activity reported thus far with very low sialidase activity. The active trans-sialidases share all the amino acids critical for the catalytic reaction with few variations in the predicted binding site for the leaving or acceptor glycan. However, these differences cannot explain the orders of magnitudes between their transfer activities, which must be due to other unidentified structural features of the proteins or substrates selectivity. Interestingly, the phylogenetic relationships between the lectin domains correlate with their specific trans-sialylation activities. This raises the question whether and how the lectin domains regulate the trans-sialidase reaction. The identification and enzymatic characterisation of the trans-sialidase family in T. congolense will contribute significantly towards the understanding of the roles of these enzymes in the pathogenesis of Animal African Trypanosomiasis.
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spelling pubmed-38550352013-12-11 Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family Gbem, Thaddeus T. Waespy, Mario Hesse, Bettina Dietz, Frank Smith, Joel Chechet, Gloria D. Nok, Jonathan A. Kelm, Sørge PLoS Negl Trop Dis Research Article Trans-sialidases are key enzymes in the life cycle of African trypanosomes in both, mammalian host and insect vector and have been associated with the disease trypanosomiasis, namely sleeping sickness and nagana. Besides the previously reported TconTS1, we have identified three additional active trans-sialidases, TconTS2, TconTS3 and TconTS4, and three trans-sialidase like genes in Trypanosoma congolense. At least TconTS1, TconTS2 and TconTS4 are found in the bloodstream of infected animals. We have characterised the enzymatic properties of recombinant proteins expressed in eukaryotic fibroblasts using fetuin as model blood glycoprotein donor substrate. One of the recombinant trans-sialidases, TconTS2, had the highest specific activity reported thus far with very low sialidase activity. The active trans-sialidases share all the amino acids critical for the catalytic reaction with few variations in the predicted binding site for the leaving or acceptor glycan. However, these differences cannot explain the orders of magnitudes between their transfer activities, which must be due to other unidentified structural features of the proteins or substrates selectivity. Interestingly, the phylogenetic relationships between the lectin domains correlate with their specific trans-sialylation activities. This raises the question whether and how the lectin domains regulate the trans-sialidase reaction. The identification and enzymatic characterisation of the trans-sialidase family in T. congolense will contribute significantly towards the understanding of the roles of these enzymes in the pathogenesis of Animal African Trypanosomiasis. Public Library of Science 2013-12-05 /pmc/articles/PMC3855035/ /pubmed/24340108 http://dx.doi.org/10.1371/journal.pntd.0002549 Text en © 2013 Gbem et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gbem, Thaddeus T.
Waespy, Mario
Hesse, Bettina
Dietz, Frank
Smith, Joel
Chechet, Gloria D.
Nok, Jonathan A.
Kelm, Sørge
Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title_full Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title_fullStr Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title_full_unstemmed Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title_short Biochemical Diversity in the Trypanosoma congolense Trans-sialidase Family
title_sort biochemical diversity in the trypanosoma congolense trans-sialidase family
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855035/
https://www.ncbi.nlm.nih.gov/pubmed/24340108
http://dx.doi.org/10.1371/journal.pntd.0002549
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