Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus
Identifieur interne : 000695 ( PascalFrancis/Corpus ); précédent : 000694; suivant : 000696Function 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 ZHUSource :
- The Journal of infectious diseases [ 0022-1899 ] ; 2005.
Descripteurs français
- Pascal (Inist)
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.
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Format Inist (serveur)
NO : | PASCAL 05-0213138 INIST |
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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:05-0213138Le document en format XML
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<author><name sortKey="Yang Zhang" sort="Yang Zhang" uniqKey="Yang Zhang" last="Yang Zhang">YANG ZHANG</name>
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<author><name sortKey="Yong Yang" sort="Yong Yang" uniqKey="Yong Yang" last="Yong Yang">YONG YANG</name>
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<author><name sortKey="Qiang Feng" sort="Qiang Feng" uniqKey="Qiang Feng" last="Qiang Feng">QIANG FENG</name>
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<author><name sortKey="Biehu Li" sort="Biehu Li" uniqKey="Biehu Li" last="Biehu Li">BIEHU LI</name>
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<author><name sortKey="Xiying Yao" sort="Xiying Yao" uniqKey="Xiying Yao" last="Xiying Yao">XIYING YAO</name>
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<author><name sortKey="Zheng Zhang" sort="Zheng Zhang" uniqKey="Zheng Zhang" last="Zheng Zhang">ZHENG ZHANG</name>
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<author><name sortKey="Ling Li" sort="Ling Li" uniqKey="Ling Li" last="Ling Li">LING LI</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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<author><name sortKey="Xiaoping Xue" sort="Xiaoping Xue" uniqKey="Xiaoping Xue" last="Xiaoping Xue">XIAOPING XUE</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Ping Zhu" sort="Ping Zhu" uniqKey="Ping Zhu" last="Ping Zhu">PING ZHU</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University</s1>
<s2>Xi'an</s2>
<s3>CHN</s3>
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<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">05-0213138</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 05-0213138 INIST</idno>
<idno type="RBID">Pascal:05-0213138</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000695</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus</title>
<author><name sortKey="Zhinan Chen" sort="Zhinan Chen" uniqKey="Zhinan Chen" last="Zhinan Chen">ZHINAN CHEN</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Li Mi" sort="Li Mi" uniqKey="Li Mi" last="Li Mi">LI MI</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</affiliation>
</author>
<author><name sortKey="Jing Xu" sort="Jing Xu" uniqKey="Jing Xu" last="Jing Xu">JING XU</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Jiyun Yu" sort="Jiyun Yu" uniqKey="Jiyun Yu" last="Jiyun Yu">JIYUN YU</name>
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</affiliation>
</author>
<author><name sortKey="Xianhui Wang" sort="Xianhui Wang" uniqKey="Xianhui Wang" last="Xianhui Wang">XIANHUI WANG</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Jianli Jiang" sort="Jianli Jiang" uniqKey="Jianli Jiang" last="Jianli Jiang">JIANLI JIANG</name>
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</author>
<author><name sortKey="Jinliang Xing" sort="Jinliang Xing" uniqKey="Jinliang Xing" last="Jinliang Xing">JINLIANG XING</name>
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</author>
<author><name sortKey="Peng Shang" sort="Peng Shang" uniqKey="Peng Shang" last="Peng Shang">PENG SHANG</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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<author><name sortKey="Airong Qian" sort="Airong Qian" uniqKey="Airong Qian" last="Airong Qian">AIRONG QIAN</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
<s3>CAN</s3>
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</author>
<author><name sortKey="Yu Li" sort="Yu Li" uniqKey="Yu Li" last="Yu Li">YU LI</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
<s3>CAN</s3>
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</author>
<author><name sortKey="Shaw, Peter X" sort="Shaw, Peter X" uniqKey="Shaw P" first="Peter X." last="Shaw">Peter X. Shaw</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Molecular Medicine, University of California, San Diego</s1>
<s2>San Diego</s2>
<s3>USA</s3>
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<s2>Beijing</s2>
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</author>
<author><name sortKey="Shumin Duan" sort="Shumin Duan" uniqKey="Shumin Duan" last="Shumin Duan">SHUMIN DUAN</name>
<affiliation><inist:fA14 i1="04"><s1>Institute of Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention</s1>
<s2>Beijing</s2>
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<author><name sortKey="Jin Ding" sort="Jin Ding" uniqKey="Jin Ding" last="Jin Ding">JIN DING</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University</s1>
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<s3>CHN</s3>
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<author><name sortKey="Chunmei Fan" sort="Chunmei Fan" uniqKey="Chunmei Fan" last="Chunmei Fan">CHUNMEI FAN</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Yang Zhang" sort="Yang Zhang" uniqKey="Yang Zhang" last="Yang Zhang">YANG ZHANG</name>
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<author><name sortKey="Yong Yang" sort="Yong Yang" uniqKey="Yong Yang" last="Yong Yang">YONG YANG</name>
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<author><name sortKey="Xiaoling Yu" sort="Xiaoling Yu" uniqKey="Xiaoling Yu" last="Xiaoling Yu">XIAOLING YU</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Qiang Feng" sort="Qiang Feng" uniqKey="Qiang Feng" last="Qiang Feng">QIANG FENG</name>
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</author>
<author><name sortKey="Biehu Li" sort="Biehu Li" uniqKey="Biehu Li" last="Biehu Li">BIEHU LI</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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<author><name sortKey="Xiying Yao" sort="Xiying Yao" uniqKey="Xiying Yao" last="Xiying Yao">XIYING YAO</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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<author><name sortKey="Zheng Zhang" sort="Zheng Zhang" uniqKey="Zheng Zhang" last="Zheng Zhang">ZHENG ZHANG</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Ling Li" sort="Ling Li" uniqKey="Ling Li" last="Ling Li">LING LI</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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<author><name sortKey="Xiaoping Xue" sort="Xiaoping Xue" uniqKey="Xiaoping Xue" last="Xiaoping Xue">XIAOPING XUE</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
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</author>
<author><name sortKey="Ping Zhu" sort="Ping Zhu" uniqKey="Ping Zhu" last="Ping Zhu">PING ZHU</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University</s1>
<s2>Xi'an</s2>
<s3>CHN</s3>
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</analytic>
<series><title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
<idno type="ISSN">0022-1899</idno>
<imprint><date when="2005">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
<idno type="ISSN">0022-1899</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Coronavirus</term>
<term>Infection</term>
<term>Microbiology</term>
<term>Severe acute respiratory syndrome</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Coronavirus</term>
<term>Microbiologie</term>
<term>Infection</term>
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><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>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0022-1899</s0>
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<fA02 i1="01"><s0>JIDIAQ</s0>
</fA02>
<fA03 i2="1"><s0>J. infect. dis.</s0>
</fA03>
<fA05><s2>191</s2>
</fA05>
<fA06><s2>5</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Function of HAbl8G/CD147 in invasion of host cells by severe acute respiratory syndrome coronavirus</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>ZHINAN CHEN</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>LI MI</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>JING XU</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>JIYUN YU</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>XIANHUI WANG</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>JIANLI JIANG</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>JINLIANG XING</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>PENG SHANG</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>AIRONG QIAN</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>YU LI</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>SHAW (Peter X.)</s1>
</fA11>
<fA11 i1="12" i2="1"><s1>JIANWEI WANG</s1>
</fA11>
<fA11 i1="13" i2="1"><s1>SHUMIN DUAN</s1>
</fA11>
<fA11 i1="14" i2="1"><s1>JIN DING</s1>
</fA11>
<fA11 i1="15" i2="1"><s1>CHUNMEI FAN</s1>
</fA11>
<fA11 i1="16" i2="1"><s1>YANG ZHANG</s1>
</fA11>
<fA11 i1="17" i2="1"><s1>YONG YANG</s1>
</fA11>
<fA11 i1="18" i2="1"><s1>XIAOLING YU</s1>
</fA11>
<fA11 i1="19" i2="1"><s1>QIANG FENG</s1>
</fA11>
<fA11 i1="20" i2="1"><s1>BIEHU LI</s1>
</fA11>
<fA11 i1="21" i2="1"><s1>XIYING YAO</s1>
</fA11>
<fA11 i1="22" i2="1"><s1>ZHENG ZHANG</s1>
</fA11>
<fA11 i1="23" i2="1"><s1>LING LI</s1>
</fA11>
<fA11 i1="24" i2="1"><s1>XIAOPING XUE</s1>
</fA11>
<fA11 i1="25" i2="1"><s1>PING ZHU</s1>
</fA11>
<fA14 i1="01"><s1>Department of Cell Biology, the Fourth Military Medical University</s1>
<s3>CAN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
<sZ>20 aut.</sZ>
<sZ>21 aut.</sZ>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
<sZ>24 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Institute of Basic Medical Sciences, Academy of Military Medical Sciences</s1>
<s3>CHN</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Molecular Medicine, University of California, San Diego</s1>
<s2>San Diego</s2>
<s3>USA</s3>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Institute of Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention</s1>
<s2>Beijing</s2>
<s3>CHN</s3>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Department of Clinical Immunology, Xijing Hospital, the Fourth Military Medical University</s1>
<s2>Xi'an</s2>
<s3>CHN</s3>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>25 aut.</sZ>
</fA14>
<fA20><s1>755-760</s1>
</fA20>
<fA21><s1>2005</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>2052</s2>
<s5>354000125691260150</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2005 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>36 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>05-0213138</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>The Journal of infectious diseases</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>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.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002A05C10</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B05</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Coronavirus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Coronavirus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Coronavirus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Microbiologie</s0>
<s5>05</s5>
</fC03>
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<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Microbiología</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Infection</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Infection</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Infección</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Syndrome respiratoire aigu sévère</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Severe acute respiratory syndrome</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Síndrome respiratorio agudo severo</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Appareil respiratoire pathologie</s0>
<s5>13</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Respiratory disease</s0>
<s5>13</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0>
<s5>13</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Virose</s0>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Viral disease</s0>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Virosis</s0>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Poumon pathologie</s0>
<s5>16</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Lung disease</s0>
<s5>16</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Pulmón patología</s0>
<s5>16</s5>
</fC07>
<fN21><s1>150</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
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<fN82><s1>OTO</s1>
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<server><NO>PASCAL 05-0213138 INIST</NO>
<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>
<DT>Publication en série; Niveau analytique</DT>
<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.</SO>
<LA>Anglais</LA>
<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>
<CC>002A05C10; 002B05</CC>
<FD>Coronavirus; Microbiologie; Infection; Syndrome respiratoire aigu sévère</FD>
<FG>Coronaviridae; Nidovirales; Virus; Appareil respiratoire pathologie; Virose; Poumon pathologie</FG>
<ED>Coronavirus; Microbiology; Infection; Severe acute respiratory syndrome</ED>
<EG>Coronaviridae; Nidovirales; Virus; Respiratory disease; Viral disease; Lung disease</EG>
<SD>Coronavirus; Microbiología; Infección; Síndrome respiratorio agudo severo</SD>
<LO>INIST-2052.354000125691260150</LO>
<ID>05-0213138</ID>
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