Fusogenic-Reactor-Based Lateral Flow Assay for Extraction-free, Multiplexed Viral RNA Detection
- Funded by European Commission
- Total publications:0 publications
Grant number: 101208836
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Key facts
Disease
COVID-19, Influenza caused by Influenza A virus subtype H1Start & end year
20252027Known Financial Commitments (USD)
$304,997.59Funder
European CommissionPrincipal Investigator
N/A
Research Location
United KingdomLead Research Institution
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORDResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Diagnostics
Special Interest Tags
Innovation
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
In this fellowship, I will leverage recent advances in membrane-fusion-based biosensor technologies to develop an extraction-free, multiplexed lateral flow assay (LFA) for rapid, home-based viral RNA detection. The COVID-19 pandemic exposed critical limitations in virus diagnostics, with antigen-based kits lacking sensitivity and specificity, while RT-qPCR tests, though accurate, are slow, resource-intensive, and impractical for widespread deployment-highlighting the urgent need for field-deployable molecular assays that deliver reliable results. Given the coexistence of multiple respiratory viruses, multiplexed detection is also crucial. This project aims to combine my expertise in membrane-fusion-based biosensor design with Professor Dame Molly Stevens' (University of Oxford) expertise in LFA-based biosensors to create a multiplex LFA system for viral RNA detection using membrane fusion approach. The system will first employ cell-mimetic fusogenic lipid vesicles (FusoLipo) encapsulating CRISPR toolkits, facilitating viral membrane fusion, RNA capture, and CRISPR-mediated detection. By utilizing two types of FusoLipo, the platform can simultaneously detect influenza A (H1N1) and SARS-CoV-2 without the need for complex RNA extraction, minimizing contamination risks. Once the vesicle's cargo is applied to the LFA, catalytic nanoparticles (Nanozyme) will amplify the signal at the detection bands, increasing sensitivity. This platform ultimately provides a accurate, and user-friendly solution for home-based multiplexed viral RNA detection. Through this fellowship, I will gain access to specialized expertise and cutting-edge facilities in lipid vesicle formulation, molecular technology, LFA development, and inorganic materials synthesis in the Stevens group, alongside advanced instrumentation to characterize vesicles at the single-particle level and further study virus-FusoLipo membrane fusion, significantly advancing my capabilities in diagnostic biosensor innovation.