Literature DB >> 20930053

Selection and application of peptide mimotopes of MPT64 protein in Mycobacterium tuberculosis.

Hua Yang1, Zhong-Hua Liu1, Li-Ting Zhang1, Jie Wang1, Huan-Seng Yang1, Lian-Hua Qin1, Rui-Liang Jin1, Yong-Hong Feng1, Zhen-Ling Cui1, Rui-Juan Zheng1, Zhong-Yi Hu1.   

Abstract

Antibody responses can be useful markers of tuberculosis (TB) infection, especially in the screening of extra-pulmonary TB. MPT64 is an important antigen in Mycobacterium tuberculosis (MTB) infection and is used in serological diagnosis. However, large variability in the diagnostic accuracy of MPT64 as a serological tool has limited its application. Phage-displayed random peptide libraries have emerged as a powerful technique to select peptides (epitopes) or mimotopes that may serve as surrogate diagnostic markers in serological tests. In the present study, this method was employed to identify mimotopes of the MPT64 protein of MTB by screening a linear heptapeptide library with rabbit antibodies raised against MPT64 protein. Two antigenic mimotopes (M2 and M6) resembling B-cell epitopes of MPT64 were identified that bound the affinity purified anti-MPT64 polyclonal antibodies and competed with MPT64 for antibody binding. From the results of sequence alignment and a structure modelling figure of MPT64, the sequence of the 2nd to 5th amino acids (DSML) of M2 was totally consistent with the sequence of the 224th to 227th amino acids of MPT64 and the peptide is located on the surface of the space structure of MPT64, suggesting that it might be a linear epitope of MPT64. The recognition of both phage-displayed and synthetic peptides of M2 by the anti-MPT64 polyclonal antibodies also supported this. Although no recurring sequence and no analogue to MPT64 of M6 were found for sequence alignment, the recognition of both phage-displayed and synthetic peptides of M6 by the anti-MPT64 polyclonal antibodies indicated that it might be a mimotope of a conformational epitope of MPT64. According to the results of the reactivity of human sera with synthetic M2 and M6 peptides and MPT64, M2 showed a significantly higher AUC and sensitivity than M6 and MPT64, especially for the sera from sputum-negative TB patients, suggesting that the M2 mimotope may be useful in serological diagnostic testing for TB.

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Year:  2010        PMID: 20930053     DOI: 10.1099/jmm.0.025098-0

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  7 in total

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Authors:  Yi Jiang; Haican Liu; Haiyin Wang; Xiangfeng Dou; Xiuqin Zhao; Yun Bai; Li Wan; Guilian Li; Wen Zhang; Chen Chen; Kanglin Wan
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3.  Dynamic evolution and immunoreactivity of aptamers binding to polyclonal antibodies against MPT64 antigen of Mycobacterium tuberculosis.

Authors:  L-H Qin; Z-H Liu; H Yang; J-L Cai; W-J Bai; J Wang; J-M Liu; Z-Y Hu
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-02-07       Impact factor: 3.267

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5.  Utility of dominant epitopes derived from cell-wall protein LppZ for immunodiagnostic of pulmonary tuberculosis.

Authors:  Jinjing Tan; Xiaoguang Wu; Suting Chen; Meng Gu; Hairong Huang; Wentao Yue
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6.  A novel B-cell epitope identified within Mycobacterium tuberculosis CFP10/ESAT-6 protein.

Authors:  Hua Yang; Haizhen Chen; Zhonghua Liu; Hui Ma; Lianhua Qin; Ruiliang Jin; Ruijuan Zheng; Yonghong Feng; Zhenling Cui; Jie Wang; Jinming Liu; Zhongyi Hu
Journal:  PLoS One       Date:  2013-01-07       Impact factor: 3.240

7.  Lysine acetylation of DosR regulates the hypoxia response of Mycobacterium tuberculosis.

Authors:  Hua Yang; Wei Sha; Zhonghua Liu; Tianqi Tang; Haipeng Liu; Lianhua Qin; Zhenling Cui; Jianxia Chen; Feng Liu; Ruijuan Zheng; Xiaochen Huang; Jie Wang; Yonghong Feng; Baoxue Ge
Journal:  Emerg Microbes Infect       Date:  2018-03-21       Impact factor: 7.163

  7 in total

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