<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>80(2)</volume><submitter>Lip KM</submitter><pubmed_abstract>We have previously shown that an Escherichia coli-expressed, denatured spike (S) protein fragment of the severe acute respiratory coronavirus, containing residues 1029 to 1192 which include the heptad repeat 2 (HR2) domain, was able to induce neutralizing polyclonal antibodies (C. T. Keng, A. Zhang, S. Shen, K. M. Lip, B. C. Fielding, T. H. Tan, C. F. Chou, C. B. Loh, S. Wang, J. Fu, X. Yang, S. G. Lim, W. Hong, and Y. J. Tan, J. Virol. 79:3289-3296, 2005). In this study, monoclonal antibodies (MAbs) were raised against this fragment to identify the linear neutralizing epitopes in the functional domain and to investigate the mechanisms involved in neutralization. Eighteen hybridomas secreting the S protein-specific MAbs were obtained. Binding sites of these MAbs were mapped to four linear </pubmed_abstract><journal>Journal of virology</journal><pagination>941-50</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1346840</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Monoclonal antibodies targeting the HR2 domain and the region immediately upstream of the HR2 of the S protein neutralize in vitro infection of severe acute respiratory syndrome coronavirus.</pubmed_title><pmcid>PMC1346840</pmcid><pubmed_authors>Oh HL</pubmed_authors><pubmed_authors>Lip KM</pubmed_authors><pubmed_authors>Li ZH</pubmed_authors><pubmed_authors>Lim SG</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Tan YJ</pubmed_authors><pubmed_authors>Mayrhofer J</pubmed_authors><pubmed_authors>Chou CF</pubmed_authors><pubmed_authors>Tan TH</pubmed_authors><pubmed_authors>Keng CT</pubmed_authors><pubmed_authors>Falkner FG</pubmed_authors><pubmed_authors>Hwang LA</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Fielding BC</pubmed_authors><pubmed_authors>Shen S</pubmed_authors><pubmed_authors>Hong W</pubmed_authors><pubmed_authors>Zhang A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Monoclonal antibodies targeting the HR2 domain and the region immediately upstream of the HR2 of the S protein neutralize in vitro infection of severe acute respiratory syndrome coronavirus.</name><description>We have previously shown that an Escherichia coli-expressed, denatured spike (S) protein fragment of the severe acute respiratory coronavirus, containing residues 1029 to 1192 which include the heptad repeat 2 (HR2) domain, was able to induce neutralizing polyclonal antibodies (C. T. Keng, A. Zhang, S. Shen, K. M. Lip, B. C. Fielding, T. H. Tan, C. F. Chou, C. B. Loh, S. Wang, J. Fu, X. Yang, S. G. Lim, W. Hong, and Y. J. Tan, J. Virol. 79:3289-3296, 2005). In this study, monoclonal antibodies (MAbs) were raised against this fragment to identify the linear neutralizing epitopes in the functional domain and to investigate the mechanisms involved in neutralization. Eighteen hybridomas secreting the S protein-specific MAbs were obtained. Binding sites of these MAbs were mapped to four linear </description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Jan</publication><modification>2025-04-19T02:22:00.883Z</modification><creation>2019-03-27T01:25:48Z</creation></dates><accession>S-EPMC1346840</accession><cross_references><pubmed>16378996</pubmed><doi>10.1128/jvi.80.2.941-950.2006</doi><doi>10.1128/JVI.80.2.941-950.2006</doi></cross_references></HashMap>