Isolation and identification of a novel WSSV nucleocapsid protein by cDNA phage display using an scFv antibody


Autoria(s): Xiao, Nan; Zhang, Xiaohua; Dai, Linfeng; Yuan, Li; Wang, Yuzhen; Zhang, Min; Xu, Tao; Dai, Heping
Data(s)

01/11/2006

Resumo

In a previous study, a scFv phage display library against white spot syndrome virus (WSSV) was constructed and yielded a clone designated A I with conformational specificity against native but not denatured viral antigen. Although the clone A1 has been used successfully as a diagnostic antibody, its precise target antigen has not been elucidated. A different strategy was adopted involving the construction of a second T7 phage display library utilizing mRNA isolated from shrimp infected with WSSV. Following RT-PCR and T7 phage library construction, phages displaying the candidate epitope were selected with A I scFv. Since successive enrichment steps were not associated with an increased titer of the phages, enrichment after successive tests was confirmed by PCR resulting in the prefer-red selection of a specific DNA sequence encoding a novel nucleocapsid protein WSSV388. Immune electron microscopy revealed that WSSV388 is located on the nucleocapsid. This result demonstrated that unknown antigen could be identified by phage display using the epitope conformation dependent scFv. (c) 2006 Elsevier B.V. All rights reserved.

In a previous study, a scFv phage display library against white spot syndrome virus (WSSV) was constructed and yielded a clone designated A I with conformational specificity against native but not denatured viral antigen. Although the clone A1 has been used successfully as a diagnostic antibody, its precise target antigen has not been elucidated. A different strategy was adopted involving the construction of a second T7 phage display library utilizing mRNA isolated from shrimp infected with WSSV. Following RT-PCR and T7 phage library construction, phages displaying the candidate epitope were selected with A I scFv. Since successive enrichment steps were not associated with an increased titer of the phages, enrichment after successive tests was confirmed by PCR resulting in the prefer-red selection of a specific DNA sequence encoding a novel nucleocapsid protein WSSV388. Immune electron microscopy revealed that WSSV388 is located on the nucleocapsid. This result demonstrated that unknown antigen could be identified by phage display using the epitope conformation dependent scFv. (c) 2006 Elsevier B.V. All rights reserved.

Identificador

http://ir.ihb.ac.cn/handle/152342/8810

http://www.irgrid.ac.cn/handle/1471x/58918

Idioma(s)

英语

Fonte

Xiao, Nan; Zhang, Xiaohua; Dai, Linfeng; Yuan, Li; Wang, Yuzhen; Zhang, Min; Xu, Tao; Dai, Heping.Isolation and identification of a novel WSSV nucleocapsid protein by cDNA phage display using an scFv antibody,JOURNAL OF VIROLOGICAL METHODS,2006,137(2):272-279

Palavras-Chave #Biochemical Research Methods; Biotechnology & Applied Microbiology; Virology #white spot syndrome virus (WSSV) #phage display #scFvAl #WSSV388
Tipo

期刊论文