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Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus

Identifieur interne : 000695 ( PascalFrancis/Corpus ); précédent : 000694; suivant : 000696

Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus

Auteurs : ZHINAN CHEN ; LI MI ; JING XU ; JIYUN YU ; XIANHUI WANG ; JIANLI JIANG ; JINLIANG XING ; PENG SHANG ; AIRONG QIAN ; YU LI ; Peter X. Shaw ; JIANWEI WANG ; SHUMIN DUAN ; JIN DING ; CHUNMEI FAN ; YANG ZHANG ; YONG YANG ; XIAOLING YU ; QIANG FENG ; BIEHU LI ; XIYING YAO ; ZHENG ZHANG ; LING LI ; XIAOPING XUE ; PING ZHU

Source :

RBID : Pascal:05-0213138

Descripteurs français

English descriptors

Abstract

To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAbl8G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAbl8G/CD147, the nu-cleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAbl8G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/ CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
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A02 01      @0 JIDIAQ
A03   1    @0 J. infect. dis.
A05       @2 191
A06       @2 5
A08 01  1  ENG  @1 Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus
A11 01  1    @1 ZHINAN CHEN
A11 02  1    @1 LI MI
A11 03  1    @1 JING XU
A11 04  1    @1 JIYUN YU
A11 05  1    @1 XIANHUI WANG
A11 06  1    @1 JIANLI JIANG
A11 07  1    @1 JINLIANG XING
A11 08  1    @1 PENG SHANG
A11 09  1    @1 AIRONG QIAN
A11 10  1    @1 YU LI
A11 11  1    @1 SHAW (Peter X.)
A11 12  1    @1 JIANWEI WANG
A11 13  1    @1 SHUMIN DUAN
A11 14  1    @1 JIN DING
A11 15  1    @1 CHUNMEI FAN
A11 16  1    @1 YANG ZHANG
A11 17  1    @1 YONG YANG
A11 18  1    @1 XIAOLING YU
A11 19  1    @1 QIANG FENG
A11 20  1    @1 BIEHU LI
A11 21  1    @1 XIYING YAO
A11 22  1    @1 ZHENG ZHANG
A11 23  1    @1 LING LI
A11 24  1    @1 XIAOPING XUE
A11 25  1    @1 PING ZHU
A14 01      @1 Department of Cell Biology, the Fourth Military Medical University @3 CAN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 8 aut. @Z 9 aut. @Z 10 aut. @Z 16 aut. @Z 17 aut. @Z 18 aut. @Z 19 aut. @Z 20 aut. @Z 21 aut. @Z 22 aut. @Z 23 aut. @Z 24 aut.
A14 02      @1 Institute of Basic Medical Sciences, Academy of Military Medical Sciences @3 CHN @Z 4 aut.
A14 03      @1 Department of Molecular Medicine, University of California, San Diego @2 San Diego @3 USA @Z 11 aut.
A14 04      @1 Institute of Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention @2 Beijing @3 CHN @Z 12 aut. @Z 13 aut.
A14 05      @1 Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University @2 Xi'an @3 CHN @Z 14 aut. @Z 15 aut. @Z 25 aut.
A20       @1 755-760
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 2052 @5 354000125691260150
A44       @0 0000 @1 © 2005 INIST-CNRS. All rights reserved.
A45       @0 36 ref.
A47 01  1    @0 05-0213138
A60       @1 P
A61       @0 A
A64 01  1    @0 The Journal of infectious diseases
A66 01      @0 USA
C01 01    ENG  @0 To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAbl8G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAbl8G/CD147, the nu-cleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAbl8G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/ CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs.
C02 01  X    @0 002A05C10
C02 02  X    @0 002B05
C03 01  X  FRE  @0 Coronavirus @2 NW @5 01
C03 01  X  ENG  @0 Coronavirus @2 NW @5 01
C03 01  X  SPA  @0 Coronavirus @2 NW @5 01
C03 02  X  FRE  @0 Microbiologie @5 05
C03 02  X  ENG  @0 Microbiology @5 05
C03 02  X  SPA  @0 Microbiología @5 05
C03 03  X  FRE  @0 Infection @5 06
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C03 03  X  SPA  @0 Infección @5 06
C03 04  X  FRE  @0 Syndrome respiratoire aigu sévère @2 NM @5 14
C03 04  X  ENG  @0 Severe acute respiratory syndrome @2 NM @5 14
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C07 02  X  FRE  @0 Nidovirales @2 NW
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C07 02  X  SPA  @0 Nidovirales @2 NW
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N21       @1 150
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 05-0213138 INIST
ET : Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus
AU : ZHINAN CHEN; LI MI; JING XU; JIYUN YU; XIANHUI WANG; JIANLI JIANG; JINLIANG XING; PENG SHANG; AIRONG QIAN; YU LI; SHAW (Peter X.); JIANWEI WANG; SHUMIN DUAN; JIN DING; CHUNMEI FAN; YANG ZHANG; YONG YANG; XIAOLING YU; QIANG FENG; BIEHU LI; XIYING YAO; ZHENG ZHANG; LING LI; XIAOPING XUE; PING ZHU
AF : Department of Cell Biology, the Fourth Military Medical University/Canada (1 aut., 2 aut., 3 aut., 5 aut., 6 aut., 7 aut., 8 aut., 9 aut., 10 aut., 16 aut., 17 aut., 18 aut., 19 aut., 20 aut., 21 aut., 22 aut., 23 aut., 24 aut.); Institute of Basic Medical Sciences, Academy of Military Medical Sciences/Chine (4 aut.); Department of Molecular Medicine, University of California, San Diego/San Diego/Etats-Unis (11 aut.); Institute of Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention/Beijing/Chine (12 aut., 13 aut.); Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University/Xi'an/Chine (14 aut., 15 aut., 25 aut.)
DT : Publication en série; Niveau analytique
SO : The Journal of infectious diseases; ISSN 0022-1899; Coden JIDIAQ; Etats-Unis; Da. 2005; Vol. 191; No. 5; Pp. 755-760; Bibl. 36 ref.
LA : Anglais
EA : To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAbl8G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAbl8G/CD147, the nu-cleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAbl8G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/ CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs.
CC : 002A05C10; 002B05
FD : Coronavirus; Microbiologie; Infection; Syndrome respiratoire aigu sévère
FG : Coronaviridae; Nidovirales; Virus; Appareil respiratoire pathologie; Virose; Poumon pathologie
ED : Coronavirus; Microbiology; Infection; Severe acute respiratory syndrome
EG : Coronaviridae; Nidovirales; Virus; Respiratory disease; Viral disease; Lung disease
SD : Coronavirus; Microbiología; Infección; Síndrome respiratorio agudo severo
LO : INIST-2052.354000125691260150
ID : 05-0213138

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Pascal:05-0213138

Le document en format XML

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<title xml:lang="en" level="a">Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus</title>
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<div type="abstract" xml:lang="en">To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAbl8G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAbl8G/CD147, the nu-cleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAbl8G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/ CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs.</div>
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<ET>Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus</ET>
<AU>ZHINAN CHEN; LI MI; JING XU; JIYUN YU; XIANHUI WANG; JIANLI JIANG; JINLIANG XING; PENG SHANG; AIRONG QIAN; YU LI; SHAW (Peter X.); JIANWEI WANG; SHUMIN DUAN; JIN DING; CHUNMEI FAN; YANG ZHANG; YONG YANG; XIAOLING YU; QIANG FENG; BIEHU LI; XIYING YAO; ZHENG ZHANG; LING LI; XIAOPING XUE; PING ZHU</AU>
<AF>Department of Cell Biology, the Fourth Military Medical University/Canada (1 aut., 2 aut., 3 aut., 5 aut., 6 aut., 7 aut., 8 aut., 9 aut., 10 aut., 16 aut., 17 aut., 18 aut., 19 aut., 20 aut., 21 aut., 22 aut., 23 aut., 24 aut.); Institute of Basic Medical Sciences, Academy of Military Medical Sciences/Chine (4 aut.); Department of Molecular Medicine, University of California, San Diego/San Diego/Etats-Unis (11 aut.); Institute of Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention/Beijing/Chine (12 aut., 13 aut.); Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University/Xi'an/Chine (14 aut., 15 aut., 25 aut.)</AF>
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<EA>To identify the function of HAb18G/CD147 in invasion of host cells by severe acute respiratory syndrome (SARS) coronavirus (CoV), we analyzed the protein-protein interaction among HAbl8G/CD147, cyclophilin A (CyPA), and SARS-CoV structural proteins by coimmunoprecipitation and surface plasmon resonance analysis. Although none of the SARS-CoV proteins was found to be directly bound to HAbl8G/CD147, the nu-cleocapsid (N) protein of SARS-CoV was bound to CyPA, which interacted with HAb18G/CD147. Further research showed that HAbl8G/CD147, a transmembrane molecule, was highly expressed on 293 cells and that CyPA was integrated with SARS-CoV. HAb18G/CD147-antagonistic peptide (AP)-9, an AP of HAb18G/CD147, had a high rate of binding to 293 cells and an inhibitory effect on SARS-CoV. These results show that HAb18G/ CD147, mediated by CyPA bound to SARS-CoV N protein, plays a functional role in facilitating invasion of host cells by SARS-CoV. Our findings provide some evidence for the cytologic mechanism of invasion by SARS-CoV and provide a molecular basis for screening anti-SARS drugs.</EA>
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