<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(4)</volume><submitter>Kim JK</submitter><pubmed_abstract>Japanese encephalitis virus (JEV), a mosquito-borne flavivirus, is closely related to West Nile (WN), yellow fever (YF), and dengue (DEN) viruses. Its plus-strand genomic RNA carries a single open reading frame encoding a polyprotein that is cleaved into three structural (C, prM/M, and E) and at least seven nonstructural (NS1/NS1', NS2A, NS2B, NS3, NS4A, NS4B, and NS5) proteins, based on previous work with WNV, YFV, and DENV. Here, we aimed to profile experimentally all the viral proteins found in JEV-infected cells. We generated a collection of 15 JEV-specific polyclonal antisera covering all parts of the viral protein-coding regions, by immunizing rabbits with 14 bacterially expressed glutathione-S-transferase fusion proteins (for all nine viral proteins except NS2B) or with a chemically</pubmed_abstract><journal>PloS one</journal><pagination>e0124318</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4410938</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Profiling of viral proteins expressed from the genomic RNA of Japanese encephalitis virus using a panel of 15 region-specific polyclonal rabbit antisera: implications for viral gene expression.</pubmed_title><pmcid>PMC4410938</pmcid><pubmed_authors>Kim JM</pubmed_authors><pubmed_authors>Yun SI</pubmed_authors><pubmed_authors>Lee YM</pubmed_authors><pubmed_authors>Kim JK</pubmed_authors><pubmed_authors>Yun GN</pubmed_authors><pubmed_authors>Song BH</pubmed_authors><pubmed_authors>Byun SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Profiling of viral proteins expressed from the genomic RNA of Japanese encephalitis virus using a panel of 15 region-specific polyclonal rabbit antisera: implications for viral gene expression.</name><description>Japanese encephalitis virus (JEV), a mosquito-borne flavivirus, is closely related to West Nile (WN), yellow fever (YF), and dengue (DEN) viruses. Its plus-strand genomic RNA carries a single open reading frame encoding a polyprotein that is cleaved into three structural (C, prM/M, and E) and at least seven nonstructural (NS1/NS1', NS2A, NS2B, NS3, NS4A, NS4B, and NS5) proteins, based on previous work with WNV, YFV, and DENV. Here, we aimed to profile experimentally all the viral proteins found in JEV-infected cells. We generated a collection of 15 JEV-specific polyclonal antisera covering all parts of the viral protein-coding regions, by immunizing rabbits with 14 bacterially expressed glutathione-S-transferase fusion proteins (for all nine viral proteins except NS2B) or with a chemically</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-04T11:05:12.459Z</modification><creation>2019-03-26T23:32:17Z</creation></dates><accession>S-EPMC4410938</accession><cross_references><pubmed>25915765</pubmed><doi>10.1371/journal.pone.0124318</doi></cross_references></HashMap>