Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homo...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2004
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/25941
- Acceso en línea:
- https://doi.org/10.1016/j.bbrc.2004.09.202
https://repository.urosario.edu.co/handle/10336/25941
- Palabra clave:
- Malaria
Plasmodium vivax
MSP8
Vaccine candidate
Surface protein
- Rights
- License
- Restringido (Acceso a grupos específicos)
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EDOCUR2 |
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Repositorio EdocUR - U. Rosario |
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8a814395-99e8-4f41-97df-12304c22be86-1bba7599d-1100-44fb-b8bf-6b76922c7da8-19db2c697-e3d4-43e1-b367-043baf7ace44-1c7b5067d-0805-42bd-ba53-04d4f30d5dd8-128469877600d191987c-6e13-4f7f-88bd-c34b437b85c6-15566b76c-9e92-4ce1-94bb-1d122c35ea36-14272869d-a644-44e9-a7a4-9c26d936bb9e-14fda4c81-5558-46e6-a038-005cc454bf3a-179653065-12020-08-06T16:20:16Z2020-08-06T16:20:16Z2004-11-26Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homologue has been identified in the present study by screening the current data obtained from this parasite’s partially sequenced genome. This new protein contains 487 amino-acids, two epidermal growth factor like domains, hydrophobic regions at the N- and C-termini compatible with a signal peptide, and a glycosylphosphatidylinositol anchor site, respectively. This gene’s transcription and its encoded protein expression have been assessed, as well as its recognition by P. vivax-infected patients’ sera. Based on this recognition, and a previous study showing that mice immunised with the Plasmodium yoelii homologous protein were protected, we consider the PvMSP8 a good candidate to be included in a multi-stage multi-antigen P. vivax vaccine.application/pdfhttps://doi.org/10.1016/j.bbrc.2004.09.202ISSN: 0006-291XEISSN: 1090-2104https://repository.urosario.edu.co/handle/10336/25941engElsevier1399No. 41393Biochemical and Biophysical Research CommunicationsVol. 324Biochemical and Biophysical Research Communications, ISSN: 0006-291X;EISSN: 1090-2104, Vol.324, No.4 (2004); pp.1393-1399https://www.sciencedirect.com/science/article/abs/pii/S0006291X04022429Restringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecBiochemical and Biophysical Research Communicationsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURMalariaPlasmodium vivaxMSP8Vaccine candidateSurface proteinPlasmodium vivax merozoite surface protein 8 cloning, expression, and characterisationPlasmodium vivax merozoite surface protein 8 clonación, expresión y caracterizaciónarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Pérez-Leal, ÓscarSierra, Adriana Y.Barrero, Carlos A.Moncada, CamiloMartínez Rángel, Diana PilarCortés, JimenaLópez, YolandaTorres, ElizabethSalazar, Luz M.Patarroyo, Manuel A.10336/25941oai:repository.urosario.edu.co:10336/259412021-06-03 00:50:21.472https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
dc.title.TranslatedTitle.spa.fl_str_mv |
Plasmodium vivax merozoite surface protein 8 clonación, expresión y caracterización |
title |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
spellingShingle |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation Malaria Plasmodium vivax MSP8 Vaccine candidate Surface protein |
title_short |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
title_full |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
title_fullStr |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
title_full_unstemmed |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
title_sort |
Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
dc.subject.keyword.spa.fl_str_mv |
Malaria Plasmodium vivax MSP8 Vaccine candidate Surface protein |
topic |
Malaria Plasmodium vivax MSP8 Vaccine candidate Surface protein |
description |
Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homologue has been identified in the present study by screening the current data obtained from this parasite’s partially sequenced genome. This new protein contains 487 amino-acids, two epidermal growth factor like domains, hydrophobic regions at the N- and C-termini compatible with a signal peptide, and a glycosylphosphatidylinositol anchor site, respectively. This gene’s transcription and its encoded protein expression have been assessed, as well as its recognition by P. vivax-infected patients’ sera. Based on this recognition, and a previous study showing that mice immunised with the Plasmodium yoelii homologous protein were protected, we consider the PvMSP8 a good candidate to be included in a multi-stage multi-antigen P. vivax vaccine. |
publishDate |
2004 |
dc.date.created.spa.fl_str_mv |
2004-11-26 |
dc.date.accessioned.none.fl_str_mv |
2020-08-06T16:20:16Z |
dc.date.available.none.fl_str_mv |
2020-08-06T16:20:16Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.bbrc.2004.09.202 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 0006-291X EISSN: 1090-2104 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/25941 |
url |
https://doi.org/10.1016/j.bbrc.2004.09.202 https://repository.urosario.edu.co/handle/10336/25941 |
identifier_str_mv |
ISSN: 0006-291X EISSN: 1090-2104 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
1399 |
dc.relation.citationIssue.none.fl_str_mv |
No. 4 |
dc.relation.citationStartPage.none.fl_str_mv |
1393 |
dc.relation.citationTitle.none.fl_str_mv |
Biochemical and Biophysical Research Communications |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 324 |
dc.relation.ispartof.spa.fl_str_mv |
Biochemical and Biophysical Research Communications, ISSN: 0006-291X;EISSN: 1090-2104, Vol.324, No.4 (2004); pp.1393-1399 |
dc.relation.uri.spa.fl_str_mv |
https://www.sciencedirect.com/science/article/abs/pii/S0006291X04022429 |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_16ec |
dc.rights.acceso.spa.fl_str_mv |
Restringido (Acceso a grupos específicos) |
rights_invalid_str_mv |
Restringido (Acceso a grupos específicos) http://purl.org/coar/access_right/c_16ec |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Elsevier |
dc.source.spa.fl_str_mv |
Biochemical and Biophysical Research Communications |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1818106718424399872 |