Generation of human antibody fragments recognizing distinct epitopes of the nucleocapsid (N) SARS-CoV protein using a phage display approach.
Identifieur interne : 002699 ( PubMed/Checkpoint ); précédent : 002698; suivant : 002700Generation of human antibody fragments recognizing distinct epitopes of the nucleocapsid (N) SARS-CoV protein using a phage display approach.
Auteurs : Michela Flego [Italie] ; Paola Di Bonito ; Alessandro Ascione ; Silvia Zamboni ; Alessandra Carattoli ; Felicia Grasso ; Antonio Cassone ; Maurizio CianfrigliaSource :
- BMC infectious diseases [ 1471-2334 ] ; 2005.
Descripteurs français
- KwdFr :
- Anticorps antiviraux (immunologie), Banque de peptides, Fragments d'immunoglobuline (immunologie), Humains, Protéines nucléocapside (), Protéines nucléocapside (génétique), Protéines nucléocapside (immunologie), Virus du SRAS (génétique), Virus du SRAS (immunologie), Épitopes (génétique), Épitopes (immunologie).
- MESH :
- génétique : Protéines nucléocapside, Virus du SRAS, Épitopes.
- immunologie : Anticorps antiviraux, Fragments d'immunoglobuline, Protéines nucléocapside, Virus du SRAS, Épitopes.
- Banque de peptides, Humains, Protéines nucléocapside.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Nucleocapsid Proteins.
- chemical , genetics : Epitopes, Nucleocapsid Proteins.
- chemical , immunology : Antibodies, Viral, Epitopes, Immunoglobulin Fragments, Nucleocapsid Proteins.
- genetics : SARS Virus.
- immunology : SARS Virus.
- Humans, Peptide Library.
Abstract
Severe acute respiratory syndrome (SARS)-CoV is a newly emerging virus that causes SARS with high mortality rate in infected people. Successful control of the global SARS epidemic will require rapid and sensitive diagnostic tests to monitor its spread, as well as, the development of vaccines and new antiviral compounds including neutralizing antibodies that effectively prevent or treat this disease.
DOI: 10.1186/1471-2334-5-73
PubMed: 16171519
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:16171519Le document en format XML
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<term>Epitopes (immunology)</term>
<term>Humans</term>
<term>Immunoglobulin Fragments (immunology)</term>
<term>Nucleocapsid Proteins (chemistry)</term>
<term>Nucleocapsid Proteins (genetics)</term>
<term>Nucleocapsid Proteins (immunology)</term>
<term>Peptide Library</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (immunology)</term>
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<term>Protéines nucléocapside ()</term>
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<term>Virus du SRAS (immunologie)</term>
<term>Épitopes (génétique)</term>
<term>Épitopes (immunologie)</term>
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<term>Nucleocapsid Proteins</term>
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<term>Epitopes</term>
<term>Immunoglobulin Fragments</term>
<term>Nucleocapsid Proteins</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>SARS Virus</term>
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<term>Virus du SRAS</term>
<term>Épitopes</term>
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<term>Fragments d'immunoglobuline</term>
<term>Protéines nucléocapside</term>
<term>Virus du SRAS</term>
<term>Épitopes</term>
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<term>Peptide Library</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS)-CoV is a newly emerging virus that causes SARS with high mortality rate in infected people. Successful control of the global SARS epidemic will require rapid and sensitive diagnostic tests to monitor its spread, as well as, the development of vaccines and new antiviral compounds including neutralizing antibodies that effectively prevent or treat this disease.</div>
</front>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16171519</PMID>
<DateCompleted><Year>2006</Year>
<Month>05</Month>
<Day>05</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1471-2334</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>5</Volume>
<PubDate><Year>2005</Year>
<Month>Sep</Month>
<Day>19</Day>
</PubDate>
</JournalIssue>
<Title>BMC infectious diseases</Title>
<ISOAbbreviation>BMC Infect. Dis.</ISOAbbreviation>
</Journal>
<ArticleTitle>Generation of human antibody fragments recognizing distinct epitopes of the nucleocapsid (N) SARS-CoV protein using a phage display approach.</ArticleTitle>
<Pagination><MedlinePgn>73</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Severe acute respiratory syndrome (SARS)-CoV is a newly emerging virus that causes SARS with high mortality rate in infected people. Successful control of the global SARS epidemic will require rapid and sensitive diagnostic tests to monitor its spread, as well as, the development of vaccines and new antiviral compounds including neutralizing antibodies that effectively prevent or treat this disease.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The human synthetic single-chain fragment variable (scFv) ETH-2 phage antibody library was used for the isolation of scFvs against the nucleocapsid (N) protein of SARS-CoV using a bio panning-based strategy. The selected scFvs were characterized under genetics-molecular aspects and for SARS-CoV N protein detection in ELISA, western blotting and immunocytochemistry.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Human scFv antibodies to N protein of SARS-CoV can be easily isolated by selecting the ETH-2 phage library on immunotubes coated with antigen. These in vitro selected human scFvs specifically recognize in ELISA and western blotting studies distinct epitopes in N protein domains and detect in immunohistochemistry investigations SARS-CoV particles in infected Vero cells.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The human scFv antibodies isolated and described in this study represent useful reagents for rapid detection of N SARS-CoV protein and SARS virus particles in infected target cells.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Flego</LastName>
<ForeName>Michela</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Drug Research and Evaluation, Istituto Superiore di Sanità, Rome, Italy. flego@iss.it</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Di Bonito</LastName>
<ForeName>Paola</ForeName>
<Initials>P</Initials>
</Author>
<Author ValidYN="Y"><LastName>Ascione</LastName>
<ForeName>Alessandro</ForeName>
<Initials>A</Initials>
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<Author ValidYN="Y"><LastName>Zamboni</LastName>
<ForeName>Silvia</ForeName>
<Initials>S</Initials>
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<ForeName>Alessandra</ForeName>
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<Author ValidYN="Y"><LastName>Grasso</LastName>
<ForeName>Felicia</ForeName>
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<Author ValidYN="Y"><LastName>Cassone</LastName>
<ForeName>Antonio</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Cianfriglia</LastName>
<ForeName>Maurizio</ForeName>
<Initials>M</Initials>
</Author>
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