SrasV1, PubMed, Checkpoint, bibRecord, 002E22

Antigenicity analysis of different regions of the severe acute respiratory syndrome coronavirus nucleocapsid protein.

Identifieur interne : 002E22 ( PubMed/Checkpoint ); précédent : 002E21; suivant : 002E23

Antigenicity analysis of different regions of the severe acute respiratory syndrome coronavirus nucleocapsid protein.

Auteurs : Zeliang Chen [République populaire de Chine] ; Decui Pei ; Lingxiao Jiang ; Yajun Song ; Jin Wang ; Hongxia Wang ; Dongsheng Zhou ; Junhui Zhai ; Zongmin Du ; Bei Li ; Maofeng Qiu ; Yanping Han ; Zhaobiao Guo ; Ruifu Yang

Source :

Clinical chemistry [ 0009-9147 ] ; 2004.

RBID : pubmed:15054081

Descripteurs français

KwdFr :
- ADN complémentaire (génétique), Analyse par réseau de protéines, Antigènes viraux (génétique), Antigènes viraux (immunologie), Clonage moléculaire, Escherichia coli (métabolisme), Humains, Protéines nucléocapside (biosynthèse), Protéines nucléocapside (génétique), Protéines nucléocapside (immunologie), Syndrome respiratoire aigu sévère (diagnostic), Virus du SRAS (immunologie), Virus du SRAS (isolement et purification), Épitopes.
MESH :
- biosynthèse : Protéines nucléocapside.
- diagnostic : Syndrome respiratoire aigu sévère.
- génétique : ADN complémentaire, Antigènes viraux, Protéines nucléocapside.
- immunologie : Antigènes viraux, Protéines nucléocapside, Virus du SRAS.
- isolement et purification : Virus du SRAS.
- métabolisme : Escherichia coli.
- Analyse par réseau de protéines, Clonage moléculaire, Humains, Épitopes.

English descriptors

KwdEn :
- Antigens, Viral (genetics), Antigens, Viral (immunology), Cloning, Molecular, DNA, Complementary (genetics), Epitopes, Escherichia coli (metabolism), Humans, Nucleocapsid Proteins (biosynthesis), Nucleocapsid Proteins (genetics), Nucleocapsid Proteins (immunology), Protein Array Analysis, SARS Virus (immunology), SARS Virus (isolation & purification), Severe Acute Respiratory Syndrome (diagnosis).
MESH :
- chemical , biosynthesis : Nucleocapsid Proteins.
- chemical , genetics : Antigens, Viral, DNA, Complementary, Nucleocapsid Proteins.
- chemical , immunology : Antigens, Viral, Nucleocapsid Proteins.
- diagnosis : Severe Acute Respiratory Syndrome.
- immunology : SARS Virus.
- isolation & purification : SARS Virus.
- metabolism : Escherichia coli.
- Cloning, Molecular, Epitopes, Humans, Protein Array Analysis.

Abstract

The widespread threat of severe acute respiratory syndrome (SARS) to human health has made urgent the development of fast and accurate analytical methods for its early diagnosis and a safe and efficient antiviral vaccine for preventive use. For this purpose, we investigated the antigenicity of different regions of the SARS coronavirus (SARS-CoV) nucleocapsid (N) protein.

DOI: 10.1373/clinchem.2004.031096
PubMed: 15054081

Affiliations:

Links toward previous steps (curation, corpus...)

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pubmed:15054081

Le document en format XML

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<term>Epitopes</term>
<term>Escherichia coli (metabolism)</term>
<term>Humans</term>
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<term>Nucleocapsid Proteins (genetics)</term>
<term>Nucleocapsid Proteins (immunology)</term>
<term>Protein Array Analysis</term>
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<term>Antigènes viraux (immunologie)</term>
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<term>Escherichia coli (métabolisme)</term>
<term>Humains</term>
<term>Protéines nucléocapside (biosynthèse)</term>
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<term>DNA, Complementary</term>
<term>Nucleocapsid Proteins</term>
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<term>Nucleocapsid Proteins</term>
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<term>Protéines nucléocapside</term>
<term>Virus du SRAS</term>
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<keywords scheme="MESH" xml:lang="en"><term>Cloning, Molecular</term>
<term>Epitopes</term>
<term>Humans</term>
<term>Protein Array Analysis</term>
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<front><div type="abstract" xml:lang="en">The widespread threat of severe acute respiratory syndrome (SARS) to human health has made urgent the development of fast and accurate analytical methods for its early diagnosis and a safe and efficient antiviral vaccine for preventive use. For this purpose, we investigated the antigenicity of different regions of the SARS coronavirus (SARS-CoV) nucleocapsid (N) protein.</div>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15054081</PMID>
<DateCompleted><Year>2004</Year>
<Month>07</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>04</Month>
<Day>03</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0009-9147</ISSN>
<JournalIssue CitedMedium="Print"><Volume>50</Volume>
<Issue>6</Issue>
<PubDate><Year>2004</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Clinical chemistry</Title>
<ISOAbbreviation>Clin. Chem.</ISOAbbreviation>
</Journal>
<ArticleTitle>Antigenicity analysis of different regions of the severe acute respiratory syndrome coronavirus nucleocapsid protein.</ArticleTitle>
<Pagination><MedlinePgn>988-95</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The widespread threat of severe acute respiratory syndrome (SARS) to human health has made urgent the development of fast and accurate analytical methods for its early diagnosis and a safe and efficient antiviral vaccine for preventive use. For this purpose, we investigated the antigenicity of different regions of the SARS coronavirus (SARS-CoV) nucleocapsid (N) protein.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The cDNA for full-length N protein and its various regions from the SARS-CoV was cloned and expressed in Escherichia coli. After purification, all of the protein fragments were printed on glass slides to fabricate a protein microarray and then probed with the sera from SARS patients to determine the reactivity of these protein fragments.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The full-length protein and two other fragments reacted with all 52 sera tested. Four important regions with possible epitopes were identified and named as EP1 (amino acids 51-71), EP2 (134-208), EP3 (249-273), and EP4 (349-422), respectively. EP2 and EP4 possessed linear epitopes, whereas EP1 and EP2 were able to form conformational epitopes that could react with most (>80%) of the tested sera. EP3 and EP4 also formed conformational epitopes, and antibodies against these epitopes existed in all 52 of the sera tested.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The N protein is a highly immunogenic protein of the SARS-CoV. Conformational epitopes are important for this protein, and antigenicity of the COOH terminus is higher than that of the NH(2) terminus. The N protein is a potential diagnostic antigen and vaccine candidate for SARS-CoV.</AbstractText>
</Abstract>
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<ForeName>Zeliang</ForeName>
<Initials>Z</Initials>
<AffiliationInfo><Affiliation>Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Pei</LastName>
<ForeName>Decui</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Jiang</LastName>
<ForeName>Lingxiao</ForeName>
<Initials>L</Initials>
</Author>
<Author ValidYN="Y"><LastName>Song</LastName>
<ForeName>Yajun</ForeName>
<Initials>Y</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wang</LastName>
<ForeName>Jin</ForeName>
<Initials>J</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wang</LastName>
<ForeName>Hongxia</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y"><LastName>Zhou</LastName>
<ForeName>Dongsheng</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Zhai</LastName>
<ForeName>Junhui</ForeName>
<Initials>J</Initials>
</Author>
<Author ValidYN="Y"><LastName>Du</LastName>
<ForeName>Zongmin</ForeName>
<Initials>Z</Initials>
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<ForeName>Bei</ForeName>
<Initials>B</Initials>
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<ForeName>Yanping</ForeName>
<Initials>Y</Initials>
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<Author ValidYN="Y"><LastName>Guo</LastName>
<ForeName>Zhaobiao</ForeName>
<Initials>Z</Initials>
</Author>
<Author ValidYN="Y"><LastName>Yang</LastName>
<ForeName>Ruifu</ForeName>
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<affiliations><list><country><li>République populaire de Chine</li>
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<name sortKey="Guo, Zhaobiao" sort="Guo, Zhaobiao" uniqKey="Guo Z" first="Zhaobiao" last="Guo">Zhaobiao Guo</name>
<name sortKey="Han, Yanping" sort="Han, Yanping" uniqKey="Han Y" first="Yanping" last="Han">Yanping Han</name>
<name sortKey="Jiang, Lingxiao" sort="Jiang, Lingxiao" uniqKey="Jiang L" first="Lingxiao" last="Jiang">Lingxiao Jiang</name>
<name sortKey="Li, Bei" sort="Li, Bei" uniqKey="Li B" first="Bei" last="Li">Bei Li</name>
<name sortKey="Pei, Decui" sort="Pei, Decui" uniqKey="Pei D" first="Decui" last="Pei">Decui Pei</name>
<name sortKey="Qiu, Maofeng" sort="Qiu, Maofeng" uniqKey="Qiu M" first="Maofeng" last="Qiu">Maofeng Qiu</name>
<name sortKey="Song, Yajun" sort="Song, Yajun" uniqKey="Song Y" first="Yajun" last="Song">Yajun Song</name>
<name sortKey="Wang, Hongxia" sort="Wang, Hongxia" uniqKey="Wang H" first="Hongxia" last="Wang">Hongxia Wang</name>
<name sortKey="Wang, Jin" sort="Wang, Jin" uniqKey="Wang J" first="Jin" last="Wang">Jin Wang</name>
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Antigenicity analysis of different regions of the severe acute respiratory syndrome coronavirus nucleocapsid protein.

Antigenicity analysis of different regions of the severe acute respiratory syndrome coronavirus nucleocapsid protein.

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