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High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles
Recombinant antigenic proteins of Toxoplasma gondii are alternative source of antigens which are easily obtainable for serodiagnosis of toxoplasmosis. In this study, highly antigenic secretory organellar proteins, dense granular GRA2 and GRA3, rhoptrial ROP2, and micronemal MIC2, were analyzed by bi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Parasitology and Tropical Medicine
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170032/ https://www.ncbi.nlm.nih.gov/pubmed/25246715 http://dx.doi.org/10.3347/kjp.2014.52.4.367 |
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author | Yang, Zhaoshou Ahn, Hye-Jin Nam, Ho-Woo |
author_facet | Yang, Zhaoshou Ahn, Hye-Jin Nam, Ho-Woo |
author_sort | Yang, Zhaoshou |
collection | PubMed |
description | Recombinant antigenic proteins of Toxoplasma gondii are alternative source of antigens which are easily obtainable for serodiagnosis of toxoplasmosis. In this study, highly antigenic secretory organellar proteins, dense granular GRA2 and GRA3, rhoptrial ROP2, and micronemal MIC2, were analyzed by bioinformatics approach to express as water-soluble forms of antigenic domains. The transmembrane region and disorder tendency of 4 secretory proteins were predicted to clone the genes into pGEX-4T-1 vector. Recombinant plasmids were transformed into BL21 (DE3) pLysS E. coli, and GST fusion proteins were expressed with IPTG. As a result, GST fusion proteins with GRA2(25-105), GRA3(39-138), ROP2(324-561), and MIC2(1-284) domains had respectively higher value of IgG avidity. The rGST-GRA2(25-105) and rGST-GRA3(39-138) were soluble, while rGST-ROP2(324-561) and rGST-MIC2(1-284) were not. GRA2(31-71), intrinsically unstructured domain (IUD) of GRA2, was used as a linker to enhance the solubility. The rGST-GRA2(31-71)-ROP2(324-561), a chimeric protein, appeared to be soluble. Moreover, rGST-GRA2(31-71)-MIC2(1-284) was also soluble and had higher IgG avidity comparing to rGST-MIC2(1-284). These 4 highly expressed and water-soluble recombinant antigenic proteins may be promising candidates to improve the serodiagnosis of toxoplasmosis in addition to the major surface antigen of SAG1. |
format | Online Article Text |
id | pubmed-4170032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society for Parasitology and Tropical Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-41700322014-09-22 High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles Yang, Zhaoshou Ahn, Hye-Jin Nam, Ho-Woo Korean J Parasitol Original Article Recombinant antigenic proteins of Toxoplasma gondii are alternative source of antigens which are easily obtainable for serodiagnosis of toxoplasmosis. In this study, highly antigenic secretory organellar proteins, dense granular GRA2 and GRA3, rhoptrial ROP2, and micronemal MIC2, were analyzed by bioinformatics approach to express as water-soluble forms of antigenic domains. The transmembrane region and disorder tendency of 4 secretory proteins were predicted to clone the genes into pGEX-4T-1 vector. Recombinant plasmids were transformed into BL21 (DE3) pLysS E. coli, and GST fusion proteins were expressed with IPTG. As a result, GST fusion proteins with GRA2(25-105), GRA3(39-138), ROP2(324-561), and MIC2(1-284) domains had respectively higher value of IgG avidity. The rGST-GRA2(25-105) and rGST-GRA3(39-138) were soluble, while rGST-ROP2(324-561) and rGST-MIC2(1-284) were not. GRA2(31-71), intrinsically unstructured domain (IUD) of GRA2, was used as a linker to enhance the solubility. The rGST-GRA2(31-71)-ROP2(324-561), a chimeric protein, appeared to be soluble. Moreover, rGST-GRA2(31-71)-MIC2(1-284) was also soluble and had higher IgG avidity comparing to rGST-MIC2(1-284). These 4 highly expressed and water-soluble recombinant antigenic proteins may be promising candidates to improve the serodiagnosis of toxoplasmosis in addition to the major surface antigen of SAG1. The Korean Society for Parasitology and Tropical Medicine 2014-08 2014-08-29 /pmc/articles/PMC4170032/ /pubmed/25246715 http://dx.doi.org/10.3347/kjp.2014.52.4.367 Text en © 2014, Korean Society for Parasitology and Tropical Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yang, Zhaoshou Ahn, Hye-Jin Nam, Ho-Woo High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title | High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title_full | High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title_fullStr | High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title_full_unstemmed | High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title_short | High Expression of Water-Soluble Recombinant Antigenic Domains of Toxoplasma gondii Secretory Organelles |
title_sort | high expression of water-soluble recombinant antigenic domains of toxoplasma gondii secretory organelles |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170032/ https://www.ncbi.nlm.nih.gov/pubmed/25246715 http://dx.doi.org/10.3347/kjp.2014.52.4.367 |
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