Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71

Objective To prepare polyclonal antisera against enterovirus 71(EV71) capsid proteins. Methods Five B cell epitope prediction softwares were used to analyze capsid proteins of EV71 and four peptides against viral protein were synthesized, VP1(aa.204-223), VP2(aa.133-163), VP3(aa.139-148+aa.173-191...

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Main Author: LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei
Format: Article
Language:zho
Published: Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2022-11-01
Series:Jichu yixue yu linchuang
Subjects:
Online Access:http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-11-1661.pdf
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author LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei
author_facet LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei
author_sort LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei
collection DOAJ
description Objective To prepare polyclonal antisera against enterovirus 71(EV71) capsid proteins. Methods Five B cell epitope prediction softwares were used to analyze capsid proteins of EV71 and four peptides against viral protein were synthesized, VP1(aa.204-223), VP2(aa.133-163), VP3(aa.139-148+aa.173-191) and VP4(aa.1-23). They were conjugated with keyhole limpet hemocyanin(KLH). BALB/c mice were subcutaneously immunized with six doses of KLH-peptides adjuvanted with MF59/CpGC274 at two-week interval. Serum sample was collected and examined with ELISA and Western blot. Results The four antisera were bound to both EV71 virus and denatured virus effectively. VP2 antiserum showed activity with denatured virus and the other three had similar binding activity to EV71 virus and denatured virus. The four antiserum samples were bound to both EV71 virus-like particle (VLP) and denatured VLP effectively. VP1 and VP2 antiserum could bind to VP1, VP0 of EV71 VLP separately. VP2 antiserum showed the highese binding activity and VP1 antiserum showed a inperior binding activity as compared to the formers. VP1 and VP2 antiserum were bound specifically and efficiently to EV71 virus. VP0 of empty particles and VP2 of intact EV71 virus particles could be simultaneously identified by VP2 antiserum. VP3 and VP4 antiserum failed to binding to no obvious binding to VLP and virus. Conclusions Four epitope peptide polyclonal antisera against EV71 are successfully prepared, which can provide ootential detection tools used in ELISA and Western blot and may be used for QC evaluation of EV71 vaccine.
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spelling doaj.art-dd03307147e94409b964105255c340aa2024-01-05T02:36:38ZzhoInstitute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.Jichu yixue yu linchuang1001-63252022-11-0142111661166610.16352/j.issn.1001-6325.2022.11.1661Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei0Department of Biophysics and Structural Biology,Institute of Basic Medical Sciences CAMS,School of Basic Medicine PUMC, Beijing 100005,ChinaObjective To prepare polyclonal antisera against enterovirus 71(EV71) capsid proteins. Methods Five B cell epitope prediction softwares were used to analyze capsid proteins of EV71 and four peptides against viral protein were synthesized, VP1(aa.204-223), VP2(aa.133-163), VP3(aa.139-148+aa.173-191) and VP4(aa.1-23). They were conjugated with keyhole limpet hemocyanin(KLH). BALB/c mice were subcutaneously immunized with six doses of KLH-peptides adjuvanted with MF59/CpGC274 at two-week interval. Serum sample was collected and examined with ELISA and Western blot. Results The four antisera were bound to both EV71 virus and denatured virus effectively. VP2 antiserum showed activity with denatured virus and the other three had similar binding activity to EV71 virus and denatured virus. The four antiserum samples were bound to both EV71 virus-like particle (VLP) and denatured VLP effectively. VP1 and VP2 antiserum could bind to VP1, VP0 of EV71 VLP separately. VP2 antiserum showed the highese binding activity and VP1 antiserum showed a inperior binding activity as compared to the formers. VP1 and VP2 antiserum were bound specifically and efficiently to EV71 virus. VP0 of empty particles and VP2 of intact EV71 virus particles could be simultaneously identified by VP2 antiserum. VP3 and VP4 antiserum failed to binding to no obvious binding to VLP and virus. Conclusions Four epitope peptide polyclonal antisera against EV71 are successfully prepared, which can provide ootential detection tools used in ELISA and Western blot and may be used for QC evaluation of EV71 vaccine.http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-11-1661.pdfenterovirus 71|vaccine|capsid protein|epitope peptide|antiserum
spellingShingle LI Chen, ZHANG Ting, WANG Zhi-rong, XU Xue-mei
Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
Jichu yixue yu linchuang
enterovirus 71|vaccine|capsid protein|epitope peptide|antiserum
title Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
title_full Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
title_fullStr Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
title_full_unstemmed Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
title_short Preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of EV71
title_sort preparation and identification of the epitope peptide polyclonal antisera against capsid proteins of ev71
topic enterovirus 71|vaccine|capsid protein|epitope peptide|antiserum
url http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-11-1661.pdf
work_keys_str_mv AT lichenzhangtingwangzhirongxuxuemei preparationandidentificationoftheepitopepeptidepolyclonalantiseraagainstcapsidproteinsofev71