Purification of Classical Swine Fever Virus E2 Subunit Vaccines Based on High Affinity Peptide Ligand
文献类型: 外文期刊
作者: Wang, Fangyu 1 ; Yu, Qiuying 2 ; Hu, Man 1 ; Xing, Guangxu 1 ; Zhao, Dong 1 ; Zhang, Gaiping 1 ;
作者机构: 1.Henan Acad Agr Sci, Henan Key Lab Anim Immunol, Zhengzhou 450002, Peoples R China
2.Henan Agr Univ, Coll Food Sci & Technol, Zhengzhou 450002, Peoples R China
3.Henan Agr Univ, Coll Anim Sci & Vet Med, Zhengzhou 450002, Peoples R China
关键词: Classical swine fever virus; glycoprotein E2; computational design; affinity peptide ligand; purification; pro-tein-peptide screening
期刊名称:PROTEIN AND PEPTIDE LETTERS ( 影响因子:1.89; 五年影响因子:1.528 )
ISSN: 0929-8665
年卷期: 2021 年 28 卷 5 期
页码:
收录情况: SCI
摘要: Background: The purification of expressed proteins is the most critical part of subunit -vaccine production. Protein-purification methods such as affinity chromatography and exchange still have the shortcomings of being time consuming and complicated. With the rapid development of computational molecular-simulation technology, structure-based peptide-ligand design has become feasible. Objection: We aimed to apply molecular docking for a peptide ligand designed for classical swine fever virus (CSFV) E2 purification. Methods: Computational-derived peptides were synthesized, and the in vitro binding interaction with E2 was investigated. The effects of purification on E2 were also evaluated. Results: The best peptide recognizing E2 was P-6, which had a sequence of KKFYWRYWEH. Based on kinetic surface plasmon resonance (SPR) analysis, the apparent affinity constant of P-6 was found to be 148 nM. Importantly, P-6 showed suitable binding affinity and specificity for E2 purification from transgenic rice seeds. Evaluation of immune antibodies in mice showed that the antibody-blocking rate on day 42 after inoculation reached 86.18% and 90.68%. Conclusion: The computational-designed peptide in this study has high sensitivity and selectivity and is thus useful for the purification of CSFV E2. The novel method of design provided a broad platform and powerful tool for protein-peptide screening, as well as new insights into CSFV vaccine design.
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