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2000
Volume 18, Issue 5
  • ISSN: 1570-162X
  • E-ISSN: 1873-4251

Abstract

Background: Finding a safe and effective vaccine for HIV-1 infection is still a major concern. Objective: This study aimed to design and produce a recombinant Nef-MPER V3 protein fused with IMT-P8 using E. coli expression system to provide a potential HIV vaccine with high cellular penetrance. Methods: After synthesizing the DNA sequence of the fusion protein, the construct was inserted into the pET-28 expression vector. The recombinant protein expression was induced using 1 mM IPTG and the product was purified through affinity chromatography. Characterization of cellular delivery, toxicity and immunogenicity of the protein was carried out. Results: The recombinant protein was expressed and confirmed by the anti-Nef antibody through western blotting. Data analyses showed that the protein possessed no considerable toxicity effect and has improved the IMT-P8 penetration rate in comparison to a control sample. Moreover, the antigen immunogenicity of the protein induced specific humoral response in mice. Conclusion: It was concluded that IMT-P8-Nef-MPER-V3 fusion protein has a high penetrance rate in mammalian cell line and low toxicity, thus it can be potentially considered as a vaccine against HIV-1.

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/content/journals/chr/10.2174/1570162X18666200612151925
2020-09-01
2025-09-28
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/content/journals/chr/10.2174/1570162X18666200612151925
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  • Article Type:
    Research Article
Keyword(s): Cell penetrating peptide; Escherichia coli; HIV-1; IMT-P8; Nef-MPER-V3; Recombinant protein
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