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http://purl.uniprot.org/citations/15790424http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15790424http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15790424http://www.w3.org/2000/01/rdf-schema#comment"

Background

The search for the dengue virus receptor has generated many candidates often identified only by molecular mass. The wide host range of the viruses in vitro combined with multiple approaches to identifying the receptor(s) has led to the notion that many receptors or attachment proteins may be involved and that the different dengue virus serotypes may utilize different receptors on the same cells as well as on different cell types.

Results

In this study we used sequential extraction of PS Clone D cell monolayers with the detergent beta-octylglucopyranoside followed by sodium deoxycholate to prepare a cell membrane-rich fraction. We then used 2 dimensional (2D) gel electrophoresis to separate the membrane proteins and applied a modified virus overlay protein binding assay (VOPBA) to show that dengue virus serotypes 1, 2 and 3 all interact with the 37 kDa/67 kDa laminin receptor (LAMR1), a common non-integrin surface protein on many cell types.

Conclusion

At least 3 of the 4 dengue serotypes interact with the 37 kDa/67 kDa laminin receptor, LAMR1, which may be a common player in dengue virus-cell surface interaction."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.org/dc/terms/identifier"doi:10.1186/1743-422x-2-25"xsd:string
http://purl.uniprot.org/citations/15790424http://purl.org/dc/terms/identifier"doi:10.1186/1743-422x-2-25"xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Cardosa M.J."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Cardosa M.J."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Jong W.W."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Jong W.W."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Tio P.H."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/author"Tio P.H."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/name"Virol. J."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/name"Virol. J."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/pages"25"xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/pages"25"xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/title"Two dimensional VOPBA reveals laminin receptor (LAMR1) interaction with dengue virus serotypes 1, 2 and 3."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/title"Two dimensional VOPBA reveals laminin receptor (LAMR1) interaction with dengue virus serotypes 1, 2 and 3."xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/volume"2"xsd:string
http://purl.uniprot.org/citations/15790424http://purl.uniprot.org/core/volume"2"xsd:string
http://purl.uniprot.org/citations/15790424http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15790424
http://purl.uniprot.org/citations/15790424http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15790424
http://purl.uniprot.org/citations/15790424http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/15790424
http://purl.uniprot.org/citations/15790424http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/15790424
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