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Mapping the Binding between the Tetraspanin Molecule (Sjc23) of Schistosoma japonicum and Human Non-Immune IgG
BACKGROUND: Schistosomal parasites can establish parasitization in a human host for decades; evasion of host immunorecognition including surface masking by acquisition of host serum components is one of the strategies explored by the parasites. Parasite molecules anchored on the membrane are the mai...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080413/ https://www.ncbi.nlm.nih.gov/pubmed/21533061 http://dx.doi.org/10.1371/journal.pone.0019112 |
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author | Wu, Chuang Cai, Pengfei Chang, Qiaocheng Hao, Lili Peng, Shuai Sun, Xiaojing Lu, Huijun Yin, Jigang Jiang, Ning Chen, Qijun |
author_facet | Wu, Chuang Cai, Pengfei Chang, Qiaocheng Hao, Lili Peng, Shuai Sun, Xiaojing Lu, Huijun Yin, Jigang Jiang, Ning Chen, Qijun |
author_sort | Wu, Chuang |
collection | PubMed |
description | BACKGROUND: Schistosomal parasites can establish parasitization in a human host for decades; evasion of host immunorecognition including surface masking by acquisition of host serum components is one of the strategies explored by the parasites. Parasite molecules anchored on the membrane are the main elements in the interaction. Sjc23, a member of the tetraspanin (TSP) family of Schistosoma japonicum, was previously found to be highly immunogenic and regarded as a vaccine candidate against schistosomiasis. However, studies indicated that immunization with Sjc23 generated rapid antibody responses which were less protective than that with other antigens. The biological function of this membrane-anchored molecule has not been defined after decades of vaccination studies. METHODOLOGY AND PRINCIPAL FINDINGS: In this study, we explored affinity pull-down and peptide competition assays to investigate the potential binding between Sjc23 molecule and human non-immune IgG. We determined that Sjc23 could bind human non-immune IgG and the binding was through the interaction of the large extra-cellular domain (LED) of Sjc23 (named Sjc23-LED) with the Fc domain of human IgG. Sjc23 had no affinity to other immunoglobulin types. Affinity precipitation (pull-down assay) in the presence of overlapping peptides further pinpointed to a 9-amino acid motif within Sjc23-LED that mediated the binding to human IgG. CONCLUSION AND SIGNIFICANCE: S. japonicum parasites cloak themselves through interaction with human non-immune IgG, and a member of the tetraspanin family, Sjc23, mediated the acquisition of human IgG via the interaction of a motif of 9 amino acids with the Fc domain of the IgG molecule. The consequence of this interaction will likely benefit parasitism of S. japonicum by evasion of host immune recognition or immunoresponses. This is the first report that an epitope of schistosomal ligand and its immunoglobulin receptor are defined, which provides further evidence of immune evasion strategy adopted by S. japonicum. |
format | Text |
id | pubmed-3080413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30804132011-04-29 Mapping the Binding between the Tetraspanin Molecule (Sjc23) of Schistosoma japonicum and Human Non-Immune IgG Wu, Chuang Cai, Pengfei Chang, Qiaocheng Hao, Lili Peng, Shuai Sun, Xiaojing Lu, Huijun Yin, Jigang Jiang, Ning Chen, Qijun PLoS One Research Article BACKGROUND: Schistosomal parasites can establish parasitization in a human host for decades; evasion of host immunorecognition including surface masking by acquisition of host serum components is one of the strategies explored by the parasites. Parasite molecules anchored on the membrane are the main elements in the interaction. Sjc23, a member of the tetraspanin (TSP) family of Schistosoma japonicum, was previously found to be highly immunogenic and regarded as a vaccine candidate against schistosomiasis. However, studies indicated that immunization with Sjc23 generated rapid antibody responses which were less protective than that with other antigens. The biological function of this membrane-anchored molecule has not been defined after decades of vaccination studies. METHODOLOGY AND PRINCIPAL FINDINGS: In this study, we explored affinity pull-down and peptide competition assays to investigate the potential binding between Sjc23 molecule and human non-immune IgG. We determined that Sjc23 could bind human non-immune IgG and the binding was through the interaction of the large extra-cellular domain (LED) of Sjc23 (named Sjc23-LED) with the Fc domain of human IgG. Sjc23 had no affinity to other immunoglobulin types. Affinity precipitation (pull-down assay) in the presence of overlapping peptides further pinpointed to a 9-amino acid motif within Sjc23-LED that mediated the binding to human IgG. CONCLUSION AND SIGNIFICANCE: S. japonicum parasites cloak themselves through interaction with human non-immune IgG, and a member of the tetraspanin family, Sjc23, mediated the acquisition of human IgG via the interaction of a motif of 9 amino acids with the Fc domain of the IgG molecule. The consequence of this interaction will likely benefit parasitism of S. japonicum by evasion of host immune recognition or immunoresponses. This is the first report that an epitope of schistosomal ligand and its immunoglobulin receptor are defined, which provides further evidence of immune evasion strategy adopted by S. japonicum. Public Library of Science 2011-04-20 /pmc/articles/PMC3080413/ /pubmed/21533061 http://dx.doi.org/10.1371/journal.pone.0019112 Text en Wu 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 Wu, Chuang Cai, Pengfei Chang, Qiaocheng Hao, Lili Peng, Shuai Sun, Xiaojing Lu, Huijun Yin, Jigang Jiang, Ning Chen, Qijun Mapping the Binding between the Tetraspanin Molecule (Sjc23) of Schistosoma japonicum and Human Non-Immune IgG |
title | Mapping the Binding between the Tetraspanin Molecule (Sjc23) of
Schistosoma japonicum and Human Non-Immune
IgG |
title_full | Mapping the Binding between the Tetraspanin Molecule (Sjc23) of
Schistosoma japonicum and Human Non-Immune
IgG |
title_fullStr | Mapping the Binding between the Tetraspanin Molecule (Sjc23) of
Schistosoma japonicum and Human Non-Immune
IgG |
title_full_unstemmed | Mapping the Binding between the Tetraspanin Molecule (Sjc23) of
Schistosoma japonicum and Human Non-Immune
IgG |
title_short | Mapping the Binding between the Tetraspanin Molecule (Sjc23) of
Schistosoma japonicum and Human Non-Immune
IgG |
title_sort | mapping the binding between the tetraspanin molecule (sjc23) of
schistosoma japonicum and human non-immune
igg |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080413/ https://www.ncbi.nlm.nih.gov/pubmed/21533061 http://dx.doi.org/10.1371/journal.pone.0019112 |
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