TY - JOUR
T1 - Expression, purification, and characterization of anti-Zika virus envelope protein
T2 - Polyclonal and chicken-derived single chain variable fragment antibodies
AU - Mwale, Pharaoh Fellow
AU - Lee, Chi Hsin
AU - Lin, Liang Tzung
AU - Leu, Sy Jye
AU - Huang, Yun Ju
AU - Chiang, Liao Chun
AU - Mao, Yan Chiao
AU - Yang, Yi Yuan
N1 - Funding Information:
Funding: This research was funded by the Ministry of Science and Technology grant number [MOST108-2622-B-038-003-CC2], the Ministry of Health and Welfare surcharge of tobacco products grant number [MOHW107-TDU-B-212-114014, and MOHW108-TDU-B-212-124014]. The APC was funded by Taipei Medical University through Yi-Yuan Yang.
Funding Information:
Acknowledgments: We thank the Ministry of Science and Technology and the Ministry of Health and Welfare surcharge of tobacco products through Yi-Yuan Yang for financial support. We also thank Tony Eight Lin for English editing and Alagie Jassey for preparing ZIKV_E DNA-transfected Vero cells for flow cytometry analysis.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/1/13
Y1 - 2020/1/13
N2 - Zika virus (ZIKV) is a new and emerging virus that has caused outbreaks worldwide. The virus has been linked to congenital neurological malformations in neonates and Guillain–Barré syndrome in adults. Currently there are no effective vaccines available. As a result, there is a great need for ZIKV treatment. In this study, we developed single chain variable fragment (scFv) antibodies that target the ZIKV envelope protein using phage display technology. We first induced an immune response in white leghorn laying hens against the ZIKV envelope (E) protein. Chickens were immunized and polyclonal immunoglobulin yolk (IgY) antibodies were extracted from egg yolks. A high-level titer of anti-ZIKV_E IgY antibodies was detected using enzyme-linked immunosorbent assay (ELISA) after the third immunization. The titer persisted for at least 9 weeks. We constructed two antibody libraries that contained 5.3 × 106 and 4.5 × 106 transformants. After biopanning, an ELISA phage assay confirmed the enrichment of specific clones. We randomly selected 26 clones that expressed ZIKV scFv antibodies and classified them into two groups, short-linker and long-linker. Of these, four showed specific binding activities toward ZIKV_E proteins. These data suggest that the polyclonal and monoclonal scFv antibodies have the diagnostic or therapeutic potential for ZIKV.
AB - Zika virus (ZIKV) is a new and emerging virus that has caused outbreaks worldwide. The virus has been linked to congenital neurological malformations in neonates and Guillain–Barré syndrome in adults. Currently there are no effective vaccines available. As a result, there is a great need for ZIKV treatment. In this study, we developed single chain variable fragment (scFv) antibodies that target the ZIKV envelope protein using phage display technology. We first induced an immune response in white leghorn laying hens against the ZIKV envelope (E) protein. Chickens were immunized and polyclonal immunoglobulin yolk (IgY) antibodies were extracted from egg yolks. A high-level titer of anti-ZIKV_E IgY antibodies was detected using enzyme-linked immunosorbent assay (ELISA) after the third immunization. The titer persisted for at least 9 weeks. We constructed two antibody libraries that contained 5.3 × 106 and 4.5 × 106 transformants. After biopanning, an ELISA phage assay confirmed the enrichment of specific clones. We randomly selected 26 clones that expressed ZIKV scFv antibodies and classified them into two groups, short-linker and long-linker. Of these, four showed specific binding activities toward ZIKV_E proteins. These data suggest that the polyclonal and monoclonal scFv antibodies have the diagnostic or therapeutic potential for ZIKV.
KW - Chicken immunization
KW - Envelope protein
KW - Immunoglobulin yolk (IgY)
KW - Phage display technology
KW - Single chain variable fragments (scFv)
KW - Zika virus (ZIKV)
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U2 - 10.3390/ijms21020492
DO - 10.3390/ijms21020492
M3 - Article
C2 - 31940993
AN - SCOPUS:85077941770
SN - 1661-6596
VL - 21
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 2
M1 - 492
ER -