Zika Virus Virus-Like Particles (VLPs)

Zika Virus Virus-Like Particles (VLPs) are engineered particles designed to mimic the structure of the Zika virus without containing its genetic material. These VLPs are primarily used in vaccine development, research, and diagnostics to combat Zika virus infections, which can cause serious health issues including congenital abnormalities and neurological disorders.

  • Structure:
    • Protein Composition: Zika VLPs typically include the major structural proteins of the virus, such as the envelope (E) protein and the membrane (prM) protein. These proteins are crucial for the virus’s ability to enter host cells and are the main targets for the immune response.
    • Envelope: The VLPs are enveloped, containing a lipid bilayer derived from the host cells used in their production. This bilayer incorporates the E and prM proteins, replicating the outer structure of the Zika virus.
  • Production:
    • Expression Systems: Zika VLPs are commonly produced using mammalian cell lines, such as HEK293 cells, to ensure proper post-translational modifications and protein folding. Insect cell lines using baculovirus vectors are also used due to their scalability and cost-effectiveness.
    • Purification: Techniques such as ultracentrifugation, affinity chromatography, and size-exclusion chromatography are employed to isolate the VLPs and ensure high purity and functionality.
  • Applications:
    • Vaccines: Zika VLPs are investigated as potential vaccine candidates because they can induce a strong immune response without the risk of causing infection. They offer a promising approach for developing vaccines that can prevent Zika virus transmission and its associated complications.
    • Research: These VLPs are used to study the structure and immunogenicity of the Zika virus, providing insights into virus-host interactions and the mechanisms of immune evasion.
    • Diagnostics: Zika VLPs can be utilized in serological assays to detect Zika-specific antibodies, aiding in the diagnosis and monitoring of Zika virus infections.
  • Immunogenicity:
    • Immune Response: Zika VLPs are designed to elicit robust immune responses by presenting the E and prM proteins in their native conformations on the particle surface. This can lead to the generation of neutralizing antibodies, providing potential protection against Zika virus.
  • Advantages:
    • Safety: VLPs contain no viral RNA, making them non-infectious and safe for use in various applications, including human vaccination.
    • Immunogenicity: The structural mimicry of the actual virus enhances the efficacy of the immune response, potentially improving vaccine effectiveness.
  • Challenges:
    • Production Complexity: The production of Zika VLPs requires sophisticated technology to maintain the structural integrity and functionality of the viral proteins.
    • Cost and Scalability: Scaling up production to meet clinical and preventative health needs can be costly and technically demanding.

AffiVLP® Zika Virus VLP (E, prM/M Proteins)
CAT# AFG-VLP-020
Size: 0.25 mg
2,832.01 2832.01 USD
AffiVLP® Zika Virus VLP (E, prM/M Proteins)
CAT# AFG-VLP-019
Size: 0.1 mg
1,501.33 1501.33 USD
AffiVLP® ZIKA VLP
CAT# AFG-VLP-327
Size: 100 µg
For Price Contact info@affigen.com 0.0 USD
AffiVLP® Zika Virus VLP (E, prM/M Proteins)
CAT# AFG-VLP-326
Size: 100 µg
For Price Contact info@affigen.com 0.0 USD
AffiVLP® Zika Virus VLP (E, prM; M Proteins)
CAT# AFG-VLP-325
Size: 100 µg
For Price Contact info@affigen.com 0.0 USD