VLP Platforms for Multipass Membrane Proteins

Advance Your Drug Discovery with VLP Display Technology 

Custom VLP Services

Membrane Protein Technology Platforms

Multipass transmembrane proteins play essential roles in cell growth, signal transduction, and intercellular communication, extensively involved in various physiological processes. They are also important targets for drug discovery and development, including research into pan-RAS inhibitor development. However, producing soluble recombinant forms of these proteins has long been a significant challenge, impeding the progress of new drug discovery.

We have developed a transmembrane protein display platform using virus-like particles (VLPs), designed for robust, functional display of full-length, multipass-transmembrane proteins in their native conformation. Our platform technology preserves the structural integrity and biological activity of the membrane proteins, enabling a broad range of applications, including immunization, antibody screening, analytical assays such as SPR, BLI and ELISA. Our transmembrane protein products undergo strict bioactivity and purity testing using SPR, ELISA, flow cytometry, and HPLC, ensuring outstanding functional performance and high batch consistency for reproducible results.

Virus-like Particle (VLP)


Virus-like particles (VLPs) are non-infectious nanoscale structures that closely mimic the organization and shape of native viruses but lack viral genetic material. They comprise self-assembled viral structural proteins and are highly immunogenic due to their repetitive, multivalent surface.

How the VLP displays transmembrane proteins.

Advantages of displaying membrane proteins on VLPs

Native-like Conformation: VLPs provide a lipid bilayer environment that helps transmembrane proteins maintain their correct folding, topology, and conformation, closely mimicking their native state on the cell membrane.

Enhanced Immunogenicity: The repetitive, multivalent display of antigens on VLPs significantly boosts immune responses compared to soluble or monomeric proteins, making them ideal for vaccine and antibody development.

Stabilization of Difficult Targets: Transmembrane proteins are often unstable or insoluble when isolated. VLPs offer structural support, increasing protein stability and solubility during purification and immunization.

Improved Antibody Generation: Presenting transmembrane proteins on VLPs enhances the likelihood of generating antibodies against conformational epitopes, which are often lost in linear peptide or denatured formats.

No Genetic Material = High Safety: VLPs are non-infectious because they lack viral genetic material, offering a safe platform for research and therapeutic development.

Product Features:

→ Mammalian cell expression system for natural folding and glycosylation

→ Strong Immunogenicity

→ Validated biological activity via ELISA and SPR

→ High batch-to-batch consistency

→ Site-specific biotinylation available

Applications:

→ Immunization

→ Antibody Screening

→ Analytical Assay Method Development and Testing

→ PK/PD studies

Product Validation

Claudin 18.2 is a tetraspanin protein family member of critical therapeutic potential for gastric and esophageal adenocarcinomas. Despite interest in drug development targeting Claudin 18.2, technical challenges in expressing high-quality Claudin 18.2 protein have significantly limited the progress of Claudin 18.2-targeted drug discovery and development. By leveraging virus-like particles, we have become the first company to successfully produce the commercially available, full-length human Claudin 18.2 protein in soluble format. Our consistent activity and purity testing results demonstrate the functional integrity and bioactivity of our VLP-displayed
protein platform.

Dynamic Light Scattering Data for KACTUS Claudin 18.2 virus-like particle (VLP) shows uniform size of the VLP membrane proteins

Figure 1. Intensity distribution of Claudin 18.2 VLPs measured by dynamic light scattering (DLS). The peak centered at approximately 150 nm indicates a homogeneous VLP particle size.

HPLC Data for KACTUS Claudin 18.2 virus-like particle (VLP) demonstrates purity of full length VLP membrane proteins for antibody drug development

Figure 2. The chromatogram shows the high-performance liquid chromatography (HPLC) profile of Claudin 18.2 VLPs, with a prominent peak observed at 4.909 minutes, indicating the retention time of the Claudin 18.2 protein. The sharp and well-defined peak suggests a high purity and consistency of the VLP preparation.

Figure 3. Immobilized Human Claudin 18.2 VLPs at 5ug/ml (100 ul/Well) on the plate. Dose response curve for Anti-Claudin 18.2 Antibody, hFc Tag with the EC50 of 6.6, 7.4, 8.3,7.3 ng/ml determined by ELISA.

Figure 4. Biotinylated Claudin 18.2 VLPs  captured on CM5 Chip via Streptavidin can bind Anti-Claudin18.2 Antibody with an affinity constant of 1.28 nM as determined in SPR assay (Biacore T200).

Available Products

Multipass Transmembrane VLP FAQs

1. In what format are the VLPs provided—liquid or lyophilized?

We offer both liquid and lyophilized formats. Lyophilization improves long-term stability and flexibility in downstream use, particularly for screening and immunization. All lyophilized batches are tested post-reconstitution to ensure bioactivity and structural integrity.

2. How is protein orientation controlled in VLPs and nanodiscs?

Proteins are expressed in mammalian systems, allowing for native folding and extracellular domain exposure. For both formats, orientation is optimized to ensure correct presentation of extracellular loops or domains, which is critical for antibody discovery and binding assays. VLPs present the extracellular domain, keeping the intracellular component out of reach within the VLP. Nanodiscs allow access to both the extra- and intracellular components, allowing you to control the protein orientation on the chip via the protein tags.

3. How many target proteins are typically displayed per VLP?

While the exact number varies by protein size and capsid packing, each VLP is engineered for high-density display. We validate the presence and consistency of surface proteins through ELISA, flow cytometry, and biophysical characterization to ensure reproducibility across batches.

4. What tags or labels are available on your membrane proteins?

Our catalog includes His-tagged, biotinylated, and fluorescent-labeled formats. These enable compatibility with a variety of workflows including SPR, BLI, ELISA, and immunoprecipitation. Tagging details are listed per product in the catalog.

5. What applications are supported by the VLP products?

These products are validated for use in immunization, ELISA,​​phage display, SPR, BLI, and PK/PD modeling. The detergent-free nature of both platforms makes them ideal for preserving native protein structure and antigenicity.

6. What quality control measures are performed on each batch?

All membrane protein products undergo batch-specific validation including size exclusion chromatography (SEC), dynamic light scattering (DLS), ELISA, and western blot (WB). This ensures batch-to-batch consistency, proper folding, and functional bioactivity. Additional QC such as SPR can be requested for a small fee.

7. What is the typical lead time for catalog vs. custom products?

Catalog products are shipped within 2–14 business days depending on stock availability. If a catalog item is in stock, we always use express overnight shipping. Custom orders typically require 6–8 weeks from project confirmation to delivery, including expression, purification, and validation.

8. How do I place an order for catalog or custom products?

Catalog items can be ordered online via credit card. For purchase orders or custom product requests, please contact us directly at orders@kactusbio.us or fill out the inquiry form on the product page.

9. Can I request data or technical validation for a specific lot?

Yes. Upon request, we provide a Certificate of Analysis (CoA) with validation data such as ELISA curves, BLI/SPR binding constants, and DLS size distribution. If needed, we can also schedule a consultation to discuss assay conditions or data interpretation.