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...
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Veröffentlicht in: | Biochemical and biophysical research communications 2004-11, Vol.324 (4), p.1393-1399 |
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container_title | Biochemical and biophysical research communications |
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creator | Perez-Leal, Oscar Sierra, Adriana Y. Barrero, Carlos A. Moncada, Camilo Martinez, Pilar Cortes, Jimena Lopez, Yolanda Torres, Elizabeth Salazar, Luz M. Patarroyo, Manuel A. |
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. |
doi_str_mv | 10.1016/j.bbrc.2004.09.202 |
format | Article |
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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.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2004.09.202</identifier><identifier>PMID: 15504368</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Motifs ; Amino Acid Sequence ; Animals ; Antibodies, Protozoan - blood ; Antigens, Protozoan - genetics ; Antigens, Protozoan - immunology ; Antigens, Protozoan - metabolism ; Cloning, Molecular ; Epidermal Growth Factor - chemistry ; Gene Expression ; Humans ; Malaria ; Molecular Sequence Data ; MSP8 ; Plasmodium falciparum ; Plasmodium vivax ; Plasmodium vivax - genetics ; Plasmodium vivax - growth & development ; Plasmodium vivax - immunology ; Plasmodium yoelii ; Protozoan Proteins - genetics ; Protozoan Proteins - immunology ; Protozoan Proteins - metabolism ; Surface protein ; Vaccine candidate</subject><ispartof>Biochemical and biophysical research communications, 2004-11, Vol.324 (4), p.1393-1399</ispartof><rights>2004 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-7d0b6569afbbda0708c9751775e487358e1677fd8b4b21cdee8e7ac0b842f0863</citedby><cites>FETCH-LOGICAL-c385t-7d0b6569afbbda0708c9751775e487358e1677fd8b4b21cdee8e7ac0b842f0863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X04022429$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15504368$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perez-Leal, Oscar</creatorcontrib><creatorcontrib>Sierra, Adriana Y.</creatorcontrib><creatorcontrib>Barrero, Carlos A.</creatorcontrib><creatorcontrib>Moncada, Camilo</creatorcontrib><creatorcontrib>Martinez, Pilar</creatorcontrib><creatorcontrib>Cortes, Jimena</creatorcontrib><creatorcontrib>Lopez, Yolanda</creatorcontrib><creatorcontrib>Torres, Elizabeth</creatorcontrib><creatorcontrib>Salazar, Luz M.</creatorcontrib><creatorcontrib>Patarroyo, Manuel A.</creatorcontrib><title>Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies, Protozoan - blood</subject><subject>Antigens, Protozoan - genetics</subject><subject>Antigens, Protozoan - immunology</subject><subject>Antigens, Protozoan - metabolism</subject><subject>Cloning, Molecular</subject><subject>Epidermal Growth Factor - chemistry</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Malaria</subject><subject>Molecular Sequence Data</subject><subject>MSP8</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium vivax</subject><subject>Plasmodium vivax - genetics</subject><subject>Plasmodium vivax - growth & development</subject><subject>Plasmodium vivax - immunology</subject><subject>Plasmodium yoelii</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - immunology</subject><subject>Protozoan Proteins - metabolism</subject><subject>Surface protein</subject><subject>Vaccine candidate</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1r3DAURUVJaCZp_0AXQaus4smTbEsydBOGJC0EkkVauhP6eG402NZUsoekvz4eZqC70NWFx7mXxyHkC4MlAyau1ktrk1tygGoJzZz8A1kwaKDgDKojsgAAUfCG_TohpzmvARirRPORnLC6hqoUakF-PnYm99GHqafbsDUvtMcU_8YwIs1Tao1DuklxxDBQRV0XhzD8vqT4skmYc4jDJTWDp-7ZJONGTCGbcb5-Iset6TJ-PuQZ-XF787T6Vtw_3H1fXd8XrlT1WEgPVtSiMa213oAE5RpZMylrrJQsa4VMSNl6ZSvLmfOICqVxYFXFW1CiPCMX-935xz8T5lH3ITvsOjNgnLIWcpbD_wNkUtUlU3wG-R50KeacsNWbFHqTXjUDvdOu13qnXe-0a2jm3JXOD-uT7dH_qxw8z8DXPYCzjG3ApLMLODj0IaEbtY_hvf03KI-UZg</recordid><startdate>20041126</startdate><enddate>20041126</enddate><creator>Perez-Leal, Oscar</creator><creator>Sierra, Adriana Y.</creator><creator>Barrero, Carlos A.</creator><creator>Moncada, Camilo</creator><creator>Martinez, Pilar</creator><creator>Cortes, Jimena</creator><creator>Lopez, Yolanda</creator><creator>Torres, Elizabeth</creator><creator>Salazar, Luz M.</creator><creator>Patarroyo, Manuel A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>20041126</creationdate><title>Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation</title><author>Perez-Leal, Oscar ; Sierra, Adriana Y. ; Barrero, Carlos A. ; Moncada, Camilo ; Martinez, Pilar ; Cortes, Jimena ; Lopez, Yolanda ; Torres, Elizabeth ; Salazar, Luz M. ; Patarroyo, Manuel A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-7d0b6569afbbda0708c9751775e487358e1677fd8b4b21cdee8e7ac0b842f0863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acid Motifs</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies, Protozoan - blood</topic><topic>Antigens, Protozoan - genetics</topic><topic>Antigens, Protozoan - immunology</topic><topic>Antigens, Protozoan - metabolism</topic><topic>Cloning, Molecular</topic><topic>Epidermal Growth Factor - chemistry</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Malaria</topic><topic>Molecular Sequence Data</topic><topic>MSP8</topic><topic>Plasmodium falciparum</topic><topic>Plasmodium vivax</topic><topic>Plasmodium vivax - genetics</topic><topic>Plasmodium vivax - growth & development</topic><topic>Plasmodium vivax - immunology</topic><topic>Plasmodium yoelii</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - immunology</topic><topic>Protozoan Proteins - metabolism</topic><topic>Surface protein</topic><topic>Vaccine candidate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perez-Leal, Oscar</creatorcontrib><creatorcontrib>Sierra, Adriana Y.</creatorcontrib><creatorcontrib>Barrero, Carlos A.</creatorcontrib><creatorcontrib>Moncada, Camilo</creatorcontrib><creatorcontrib>Martinez, Pilar</creatorcontrib><creatorcontrib>Cortes, Jimena</creatorcontrib><creatorcontrib>Lopez, Yolanda</creatorcontrib><creatorcontrib>Torres, Elizabeth</creatorcontrib><creatorcontrib>Salazar, Luz M.</creatorcontrib><creatorcontrib>Patarroyo, Manuel A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perez-Leal, Oscar</au><au>Sierra, Adriana Y.</au><au>Barrero, Carlos A.</au><au>Moncada, Camilo</au><au>Martinez, Pilar</au><au>Cortes, Jimena</au><au>Lopez, Yolanda</au><au>Torres, Elizabeth</au><au>Salazar, Luz M.</au><au>Patarroyo, Manuel A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2004-11-26</date><risdate>2004</risdate><volume>324</volume><issue>4</issue><spage>1393</spage><epage>1399</epage><pages>1393-1399</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15504368</pmid><doi>10.1016/j.bbrc.2004.09.202</doi><tpages>7</tpages></addata></record> |
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subjects | Amino Acid Motifs Amino Acid Sequence Animals Antibodies, Protozoan - blood Antigens, Protozoan - genetics Antigens, Protozoan - immunology Antigens, Protozoan - metabolism Cloning, Molecular Epidermal Growth Factor - chemistry Gene Expression Humans Malaria Molecular Sequence Data MSP8 Plasmodium falciparum Plasmodium vivax Plasmodium vivax - genetics Plasmodium vivax - growth & development Plasmodium vivax - immunology Plasmodium yoelii Protozoan Proteins - genetics Protozoan Proteins - immunology Protozoan Proteins - metabolism Surface protein Vaccine candidate |
title | Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation |
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