Identification of an epitope of SARS-coronavirus nucleocapsid protein

被引:69
|
作者
Lin, Y
Shen, X
Yang, RF
Li, YX
Ji, YY
He, YY
Shi, MD
Lu, W
Shi, TL
Wang, J
Wang, HX
Jiang, HL
Shen, JH
Xie, YH
Wang, Y
Pei, G
Shen, BF
Wu, JR [1 ]
Sun, B
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Inst Mat Med,Bioinformat Ctr, Shanghai 200031, Peoples R China
[2] Acad Mil Med Sci, Inst Basic Med Sci, Inst Microbiol & Epidemiol, Beijing 100071, Peoples R China
关键词
severe acute respiratory syndrome-coronavirus; necleocapsid protein; epitope; polyclonal antibody; antiserum;
D O I
10.1038/sj.cr.7290158
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The nucleocapsid (N) protein of severe acute respiratory syndrome-coronavirus (SARS-CoV) is a major virion structural protein. In this study, two epitopes (N1 and N2) of the N protein of SARS-CoV were predicted by bioinformatics analysis. After immunization with two peptides, the peptides-specific antibodies were isolated from the immunized rabbits. The further experiments demonstrated that N1 peptide-induced polyclonal antibodies had a high affinity to bind to E. coli expressed N protein of SARS-CoV. Furthermore, it was confirmed that N1 peptide-specific IgG antibodies were detectable in the sera of severe acute respiratory syndrome (SARS) patients. The results indicated that an epitope of the N protein has been identified and N protein specific Abs were produced by peptide immunization, which will be useful for the study of SARS-Cov.
引用
收藏
页码:141 / 145
页数:5
相关论文
共 50 条
  • [31] Nucleocapsid protein of SARS coronavirus tightly binds to human cyclophilin A
    Luo, C
    Luo, HB
    Zheng, SX
    Gui, CS
    Yue, LD
    Yu, CY
    Sun, T
    He, PL
    Chen, J
    Shen, JH
    Luo, XM
    Li, YX
    Liu, H
    Bai, DL
    Shen, JK
    Yang, YM
    Li, FQ
    Zuo, JP
    Hilgenfeld, R
    Pei, G
    Chen, KX
    Shen, X
    Jiang, HL
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 321 (03) : 557 - 565
  • [32] Candidate Genes Associated with Susceptibility for SARS-Coronavirus
    Hsieh, Ying-Hen
    Chen, Cathy W. S.
    Schmitz, Shu-Fang Hsu
    King, Chwan-Chuan
    Chen, Wei-Ju
    Wu, Yi-Chun
    Ho, Mei-Shang
    BULLETIN OF MATHEMATICAL BIOLOGY, 2010, 72 (01) : 122 - 132
  • [33] Characterization and inhibition of SARS-coronavirus main protease
    Liang, Po-Huang
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2006, 6 (04) : 361 - 376
  • [34] Determination of SARS-coronavirus by a microfluidic chip system
    Zhou, ZM
    Liu, DY
    Zhong, RT
    Dai, ZP
    Wu, DP
    Wang, H
    Du, YG
    Xia, ZN
    Zhang, LP
    Mei, XD
    Lin, BC
    ELECTROPHORESIS, 2004, 25 (17) : 3032 - 3039
  • [35] Structure and intracellular targeting of the SARS-coronavirus Orf7a accessory protein
    Nelson, CA
    Pekosz, A
    Lee, CA
    Diamond, MS
    Fremont, DH
    STRUCTURE, 2005, 13 (01) : 75 - 85
  • [36] Close relationship between SARS-coronavirus and group 2 coronavirus
    Kim, OJ
    Lee, DH
    Lee, CH
    JOURNAL OF MICROBIOLOGY, 2006, 44 (01) : 83 - 91
  • [37] Candidate Genes Associated with Susceptibility for SARS-Coronavirus
    Ying-Hen Hsieh
    Cathy W. S. Chen
    Shu-Fang Hsu Schmitz
    Chwan-Chuan King
    Wei-Ju Chen
    Yi-Chun Wu
    Mei-Shang Ho
    Bulletin of Mathematical Biology, 2010, 72 : 122 - 132
  • [38] Advancements in the development of antivirals against SARS-Coronavirus
    Kumar, Mrityunjay
    Baig, Mirza Sarwar
    Bhardwaj, Kanchan
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2025, 15
  • [39] Wildlife hosts of SARS-coronavirus and related viruses
    Wang, L-F.
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2007, 29 : S80 - S80
  • [40] SARS diagnosis, monitoring and prognostication by SARS-coronavirus RNA detection
    Lo, Y. M. D.
    HONG KONG MEDICAL JOURNAL, 2009, 15 (06) : 11 - 14