hantaan virus s gene 5 end of 311bp encoding prokaryotic protein expression purification and antigenicity of the(hantaan病毒s基因5 311年底bp编码原核的蛋白质表达纯化和抗原性).docVIP
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hantaan virus s gene 5 end of 311bp encoding prokaryotic protein expression purification and antigenicity of the(hantaan病毒s基因5 311年底bp编码原核的蛋白质表达纯化和抗原性)
Hantaan virus S gene 5 ‘end of 311bp encoding prokaryotic protein expression purification and antigenicity of the
To write thesis net: Author: Yong Zhi-Kai Xu Yan rock Zhangfang Lin Wang Haitao Xue Xiaoping TGF -
[Keywords] Hantaan virus Keywords: Hantaan virus; nucleoprotein; prokaryotic expression; purification; antigenic sites Abstract: Objective To further understand the Hantaan virus nucleoprotein amino end of antigenic characteristics. Methods build Hantaan virus S gene 5 ‘end of the 311bp fragment of the original expression vector, and induced the expression and purification of Mr. 3.6 ?104 of the fusion protein (Hantaan virus nuclear protein amino terminus Mr 1.0 ?104 and Mr 2.6 ?104 GST fusion; identified antigenic sito fes of the protein mAb, Western-blot and ELISA results only partially complete nucleoprotein mAb Mr 3.6 ?104 fusion protein reaction nucleoprotein amino terminus Mr 2.6 ?104 fragment reaction mAbs (1A8, A35, 8E8, 3A9, 3G11) can with Mr 3.6 ?104 fusion pr otein reaction. conclusion Hantaan virus nuclear The presence of one or several linear epitope in the protein amino-terminal Mr less than 1.0 ?104, and the carboxy terminus may be mainly plays a role in maintaining the integrity nucleoprotein dimensional conformation, and influence the identification perspective epitope of mAb with the binding of the protein.
Keywords: hataan virus; nucleoprotein; prokayotic expres-sion; purification; antigentic epitope
Abstract: AIM To further understand the antigen charac-teristic of the amino proximal of hantaan virus nucleoprotein.METHODS We constructed the prokaryotic vector of han-taan S gene5’-terminal311bp, then inducingly expressed and purified the Mr 3.6 ?104 fusion protein.Then , we further identified its antigentic epitopes by Western blot and ELISA methods using the nucleoprotein specific mAbs.RESULTS We detected that only parts of mAbs freacting with integrated nucleoprotein could react with Mr 3.6 ?104 fusion protein, and
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