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[The expression and activity detection of a variant N protein of SARS-CoV].

Identifieur interne : 002D13 ( PubMed/Corpus ); précédent : 002D12; suivant : 002D14

[The expression and activity detection of a variant N protein of SARS-CoV].

Auteurs : Yang Qi ; Yu Zheng ; Cui-Li Shu ; Li Jiang ; Yan Hu ; Pan-Yong Mao ; Yun Cheng

Source :

RBID : pubmed:15207085

English descriptors

Abstract

To construct an expression vector pGEX-2T/N, and to express the fusion protein consisting of N protein of SARS-CoV and GST in E.coli.

PubMed: 15207085

Links to Exploration step

pubmed:15207085

Le document en format XML

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<title xml:lang="en">[The expression and activity detection of a variant N protein of SARS-CoV].</title>
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<name sortKey="Qi, Yang" sort="Qi, Yang" uniqKey="Qi Y" first="Yang" last="Qi">Yang Qi</name>
<affiliation>
<nlm:affiliation>Department of Immunology, Institute of Infectious Diseases, 302th Hospital of PLA, Beijing 100039, China. qiy2004@sohu.com</nlm:affiliation>
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<name sortKey="Zheng, Yu" sort="Zheng, Yu" uniqKey="Zheng Y" first="Yu" last="Zheng">Yu Zheng</name>
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<name sortKey="Shu, Cui Li" sort="Shu, Cui Li" uniqKey="Shu C" first="Cui-Li" last="Shu">Cui-Li Shu</name>
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<name sortKey="Jiang, Li" sort="Jiang, Li" uniqKey="Jiang L" first="Li" last="Jiang">Li Jiang</name>
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<name sortKey="Hu, Yan" sort="Hu, Yan" uniqKey="Hu Y" first="Yan" last="Hu">Yan Hu</name>
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<name sortKey="Mao, Pan Yong" sort="Mao, Pan Yong" uniqKey="Mao P" first="Pan-Yong" last="Mao">Pan-Yong Mao</name>
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<name sortKey="Cheng, Yun" sort="Cheng, Yun" uniqKey="Cheng Y" first="Yun" last="Cheng">Yun Cheng</name>
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<term>Escherichia coli (metabolism)</term>
<term>Genetic Vectors</term>
<term>Glutathione Transferase (genetics)</term>
<term>Humans</term>
<term>Nucleocapsid Proteins (biosynthesis)</term>
<term>Nucleocapsid Proteins (genetics)</term>
<term>Nucleocapsid Proteins (immunology)</term>
<term>Recombinant Fusion Proteins (biosynthesis)</term>
<term>Recombinant Fusion Proteins (genetics)</term>
<term>Recombinant Fusion Proteins (immunology)</term>
<term>SARS Virus (genetics)</term>
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<term>Nucleocapsid Proteins</term>
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<term>Glutathione Transferase</term>
<term>Nucleocapsid Proteins</term>
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<term>Escherichia coli</term>
<term>SARS Virus</term>
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<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Nucleocapsid Proteins</term>
<term>Recombinant Fusion Proteins</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Escherichia coli</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Base Sequence</term>
<term>Genetic Vectors</term>
<term>Humans</term>
<term>Sequence Deletion</term>
<term>Transfection</term>
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<front>
<div type="abstract" xml:lang="en">To construct an expression vector pGEX-2T/N, and to express the fusion protein consisting of N protein of SARS-CoV and GST in E.coli.</div>
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<AbstractText Label="AIM" NlmCategory="OBJECTIVE">To construct an expression vector pGEX-2T/N, and to express the fusion protein consisting of N protein of SARS-CoV and GST in E.coli.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The N region gene of SARS-CoV was cloned by RT-PCR. The expression vector was constructed by DNA recombination. The recombinant plasmid was transformed into E.coli BL21(DE3). The expression of the fusion protein was detected by Western blot.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">(1) As compared with the sequences in GenBank, 20 bp were deleted in DNA sequence of the cloned N protein. (2) The fusion protein GST-N was soluble. Western blot analysis showed that the reaction of GST-N to anti-SARS-CoV sera was positive.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The pGEX-2T/N has been constructed and expressed in the form of fusion protein GST-N successfully, which lays the foundation for further study of SARS-CoV N protein.</AbstractText>
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