Nipah Virus(NiV)Research Proteins
NiV Research Tools
Full-length Proteins •Vaccine Antigens •Therapeutic Antibody Development
Nipah virus(NiV)is a highly pathogenic zoonotic RNA virus with a fatality rate of 40-75%, listed as a WHO priority pathogen.Creative BioMart offers validated Pre-F, Post-F trimers, G protein, and N protein antigens to accelerate next-generation vaccine(mRNA-1215, ChAdOx1)and monoclonal antibody(m102.4)development.

Need custom proteins or proteins from specific species?
We offer custom expression services for wild-type/mutant NiV proteins, including site-directed mutagenesis(such as F protein stabilization mutations L104C/I114C), special tags(Fc/Avi/Biotin), and large-scale GMP pre-production services.
Latest Research&Vaccine Development
1Clinical Vaccine Platforms
mRNA-1215 Vaccine(Moderna/NIAID)
- Status: Phase 1 Ongoing
- Description: mRNA vaccine encoding stabilized Pre-F and G proteins using LNP technology
- Key Data: 2024 Hendra@30 meeting shows cross-neutralization of NiV and HeV in vaccinated subjects
- Trial ID: NCT05398796
- Strategy: Prime-Boost
ChAdOx1 NiV-B(Oxford University/CEPI)
- Status: Phase 1 Recruiting
- Description: Chimpanzee adenovirus vector expressing NiV-B G protein
- Key Data: Complete protection in hamster models against Bangladesh strain(100%fatal)
- Trial ID: ISRCTN87634044
- Platform: Adenoviral Vector
HenipaVax™(Auro Vaccines)
- Status: Phase 1 Complete
- Description: Subunit vaccine based on HeV soluble G protein(sG)with alum adjuvant
- Key Data: Cross-protection with NiV(81%G protein homology)
- Trial ID: NCT04199169
- Platform: Protein Subunit
rVSV-NiV(Crozet BioPharma)
- Status: Phase 1 Ongoing
- Description: Recombinant vesicular stomatitis virus vector expressing NiV-M G protein(PHV02)
- Key Data: Single-dose rapid protection in non-human primates for emergency response
- Trial ID: NCT05178901
- Feature: Single-Dose
2Structural Biology Advances
Pre-F Stabilization Technology
2024 structural studies show Pre-Fusion conformation induces stronger neutralizing antibodies than Post-Fusion.Disulfide bonds(L104C/I114C)and cavity-filling mutations(L172F, S191P)lock F protein in pre-fusion state, exposing critical neutralizing epitopes(e.g., mAb66 binding site).
Key Technologies:
G Protein Tetramer Structure
Cryo-EM reveals NiV G protein forms homotetramers(120×200Å)with four-helix bundle stalks andβ-propeller head domains.Non-competitive antibody combinations(e.g., nAH1.3+m102.4)show synergistic effects, reducing escape mutation risks.
Key Features:
Therapeutic mAb m102.4
The only NiV therapeutic in clinical trials.Treatment on day 5 post-infection achieves 100%survival in NHPs(clinical stage).Targets G protein receptor-binding site with cross-neutralizing activity against NiV and HeV.
Emerging Henipavirus Threats(2024 Update)
Beyond NiV and HeV, newly discovered viruses pose additional threats:
These viruses share F/G glycoprotein structures and Ephrin-B2 receptor usage—our NiV proteins enable cross-virus research for prototype pathogen preparedness.
Applications&Solutions
Vaccine Development
- Subunit vaccine immunogens
- mRNA vaccine validation
- Neutralizing antibody titers
- Pseudovirus neutralization
Antibody Therapeutics
- Therapeutic mAb screening(e.g., m102.4 analogs)
- Bispecific antibody design
- Epitope mapping
- Cross-reactivity assessment
Diagnostics
- ELISA antigens(NP protein)
- Immunofluorescence assays
- Lateral flow devices
- Serological surveys
Structural Biology
- Cryo-EM sample preparation
- Receptor binding studies(Ephrin-B2)
- Fusion mechanism analysis
- Small molecule screening
Quality Assurance
Multi-dimensional Purity Verification
- SEC-HPLC(Size Exclusion Chromatography)for aggregates and fragments
- SDS-PAGE for molecular weight verification
- LAL endotoxin testing: <0.1 EU/μg(Vaccine Grade: <0.01 EU/μg)
Bioactivity Validation
- G Protein: Ephrin-B2 binding ELISA(EC50 validation)
- F Protein: Pre-F specific mAb(e.g., mAb66)binding verification
- COA and activity data provided with all batches
Conformational Specificity Guarantee
Pre-F proteins use DS-Cav1 stabilization design, verified by negative-stain EM and specific antibodies(e.g., DS7)to prevent spontaneous Post-Fusion conversion.
Quality Metrics:
Accelerate Nipah Virus Medical Countermeasures
Whether developing mRNA vaccines, therapeutic antibodies, or diagnostic reagents, our high-quality recombinant proteins provide reliable support for your research. Contact our technical team today for samples and custom solutions.
Service Guarantees: Global Shipping | Technical Support | Batch-to-Batch Consistency | Custom Services Available
Resources
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Understanding Nipah Virus Entry: The Deadly Dance of Proteins G and F
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Pre-F vs. Post-F: Choosing the Right Antigen for Your NiV Research
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Troubleshooting Guide: Optimizing Signal-to-Noise Ratio in NiV ELISA
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Brief introduction to Nipah virus
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2026 Nipah Vaccine Race: Who is Leading?
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