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Amino acids 1055 to 1192 in the S2 region of severe acute respiratory syndrome coronavirus S protein induce neutralizing antibodies : Implications for the development of vaccines and antiviral agents

Identifieur interne : 000278 ( PascalFrancis/Curation ); précédent : 000277; suivant : 000279

Amino acids 1055 to 1192 in the S2 region of severe acute respiratory syndrome coronavirus S protein induce neutralizing antibodies : Implications for the development of vaccines and antiviral agents

Auteurs : Choong-Tat Keng [Singapour] ; AIHUA ZHANG [République populaire de Chine] ; SHUO SHEN [Singapour] ; Kuo-Ming Lip [Singapour] ; Burtram C. Fielding [Singapour] ; Timothy H. P. Tan [Singapour] ; Chih-Fong Chou [Singapour] ; CHAY BOON LOH [Singapour] ; SIFANG WANG [Singapour] ; JIANLIN FU [Singapour] ; XIAOMING YANG [République populaire de Chine] ; SENG GEE LIM [Singapour] ; WANJIN HONG [Singapour] ; Yee-Joo Tan [Singapour]

Source :

RBID : Pascal:05-0158491

Descripteurs français

English descriptors

Abstract

The spike (S) protein of the severe acute respiratory syndrome coronavirus (SARS-CoV) interacts with cellular receptors to mediate membrane fusion, allowing viral entry into host cells; hence it is recognized as the primary target of neutralizing antibodies, and therefore knowledge of antigenic determinants that can elicit neutralizing antibodies could be beneficial for the development of a protective vaccine. Here, we expressed five different fragments of S, covering the entire ectodomain (amino acids 48 to 1192), as glutathione S-transferase fusion proteins in Escherichia coli and used the purified proteins to raise antibodies in rabbits. By Western blot analysis and immunoprecipitation experiments, we showed that all the antibodies are specific and highly sensitive to both the native and denatured forms of the full-length S protein expressed in virus-infected cells and transfected cells, respectively. Indirect immunofluorescence performed on fixed but unpermeabilized cells showed that these antibodies can recognize the mature form of S on the cell surface. All the antibodies were also able to detect the maturation of the 200-kDa form of S to the 210-kDa form by pulse-chase experiments. When the antibodies were tested for their ability to inhibit SARS-CoV propagation in Vero E6 culture, it was found that the anti-SΔ10 antibody, which was targeted to amino acid residues 1029 to 1192 of S, which include heptad repeat 2, has strong neutralizing activities, suggesting that this region of S carries neutralizing epitopes and is very important for virus entry into cells.
pA  
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A03   1    @0 J. virol.
A05       @2 79
A06       @2 6
A08 01  1  ENG  @1 Amino acids 1055 to 1192 in the S2 region of severe acute respiratory syndrome coronavirus S protein induce neutralizing antibodies : Implications for the development of vaccines and antiviral agents
A11 01  1    @1 KENG (Choong-Tat)
A11 02  1    @1 AIHUA ZHANG
A11 03  1    @1 SHUO SHEN
A11 04  1    @1 LIP (Kuo-Ming)
A11 05  1    @1 FIELDING (Burtram C.)
A11 06  1    @1 TAN (Timothy H. P.)
A11 07  1    @1 CHOU (Chih-Fong)
A11 08  1    @1 CHAY BOON LOH
A11 09  1    @1 SIFANG WANG
A11 10  1    @1 JIANLIN FU
A11 11  1    @1 XIAOMING YANG
A11 12  1    @1 SENG GEE LIM
A11 13  1    @1 WANJIN HONG
A11 14  1    @1 TAN (Yee-Joo)
A14 01      @1 Institute of Molecular and Cell Biology @3 SGP @Z 1 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 8 aut. @Z 9 aut. @Z 10 aut. @Z 12 aut. @Z 13 aut. @Z 14 aut.
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A60       @1 P
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A64 01  1    @0 Journal of virology
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C01 01    ENG  @0 The spike (S) protein of the severe acute respiratory syndrome coronavirus (SARS-CoV) interacts with cellular receptors to mediate membrane fusion, allowing viral entry into host cells; hence it is recognized as the primary target of neutralizing antibodies, and therefore knowledge of antigenic determinants that can elicit neutralizing antibodies could be beneficial for the development of a protective vaccine. Here, we expressed five different fragments of S, covering the entire ectodomain (amino acids 48 to 1192), as glutathione S-transferase fusion proteins in Escherichia coli and used the purified proteins to raise antibodies in rabbits. By Western blot analysis and immunoprecipitation experiments, we showed that all the antibodies are specific and highly sensitive to both the native and denatured forms of the full-length S protein expressed in virus-infected cells and transfected cells, respectively. Indirect immunofluorescence performed on fixed but unpermeabilized cells showed that these antibodies can recognize the mature form of S on the cell surface. All the antibodies were also able to detect the maturation of the 200-kDa form of S to the 210-kDa form by pulse-chase experiments. When the antibodies were tested for their ability to inhibit SARS-CoV propagation in Vero E6 culture, it was found that the anti-SΔ10 antibody, which was targeted to amino acid residues 1029 to 1192 of S, which include heptad repeat 2, has strong neutralizing activities, suggesting that this region of S carries neutralizing epitopes and is very important for virus entry into cells.
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C03 02  X  FRE  @0 Protéine @5 05
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C03 02  X  SPA  @0 Proteína @5 05
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N21       @1 108
N44 01      @1 OTO
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Pascal:05-0158491

Le document en format XML

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<div type="abstract" xml:lang="en">The spike (S) protein of the severe acute respiratory syndrome coronavirus (SARS-CoV) interacts with cellular receptors to mediate membrane fusion, allowing viral entry into host cells; hence it is recognized as the primary target of neutralizing antibodies, and therefore knowledge of antigenic determinants that can elicit neutralizing antibodies could be beneficial for the development of a protective vaccine. Here, we expressed five different fragments of S, covering the entire ectodomain (amino acids 48 to 1192), as glutathione S-transferase fusion proteins in Escherichia coli and used the purified proteins to raise antibodies in rabbits. By Western blot analysis and immunoprecipitation experiments, we showed that all the antibodies are specific and highly sensitive to both the native and denatured forms of the full-length S protein expressed in virus-infected cells and transfected cells, respectively. Indirect immunofluorescence performed on fixed but unpermeabilized cells showed that these antibodies can recognize the mature form of S on the cell surface. All the antibodies were also able to detect the maturation of the 200-kDa form of S to the 210-kDa form by pulse-chase experiments. When the antibodies were tested for their ability to inhibit SARS-CoV propagation in Vero E6 culture, it was found that the anti-SΔ10 antibody, which was targeted to amino acid residues 1029 to 1192 of S, which include heptad repeat 2, has strong neutralizing activities, suggesting that this region of S carries neutralizing epitopes and is very important for virus entry into cells.</div>
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