In silico Analysis and Modeling of ACP-MIP–PilQ Chimeric Antigen from Neisseria meningitidis Serogroup B

نویسندگان

  • Abazar Pournajaf Department of Microbiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  • Alireza Salimi Chirani Department of Microbiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Gholamreza Irajian Department of Microbiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  • Mansour Sedighi Department of Microbiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  • Masoud Tohidfar Agricultural Biotechnology Research Institute of Iran, Tehran, Iran
  • Mehrdad Gholami Department of Microbiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  • Mona Moshiri Department of Pathobiology, Division of Microbiology, Faculty of Public Health, Tehran University of Medical Sciences, Tehran, Iran
چکیده مقاله:

Background: Neisseria meningitidis, a life-threatening human pathogen with the potential to cause large epidemics, can be isolated from the nasopharynx of 5–15% of adults. The aim of the current study was to evaluate biophysical and biochemical properties and immunological aspects of chimeric acyl-carrier protein-macrophage infectivity potentiator protein-type IV pilus biogenesis protein antigen (ACP-MIP-PilQ) from N. meningitidis serogroup B strain. Methods: Biochemical properties and multiple alignments were predicted by appropriate web servers. Secondary molecular structures were predicted based on Chou and Fasman, Garnier-Osguthorpe-Robson, and Neural Network methods. Tertiary modeling elucidated conformational properties of the chimeric protein. Proteasome cleavage and transporter associated with antigen processing (TAP) binding sites, and T- and B-cell antigenic epitopes, were predicted using bioinformatic web servers. Results: Based on our in silico and immunoinformatics analyses, the ACP-MIP-PilQ protein (AMP) can induce high-level cross-strain bactericidal activity. In addition, several immune proteasomal cleavage sites were detected. The 22 epitopes associated with MHC class I and class II (DR) alleles were confirmed in the AMP. Thirty linear B-cell epitopes as antigenic regions were predicted from the full-length protein. Conclusion: All predicted properties of the AMP indicate it could be a good candidate for further immunological in vitro and in vivo studies.

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in silico analysis and modeling of acp-mip–pilq chimeric antigen from neisseria meningitidis serogroup b

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عنوان ژورنال

دوره 4  شماره 1

صفحات  50- 59

تاریخ انتشار 2015-10

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