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huang, X.

Publications and source records attributed to huang, X..

2 recordsLinked to original sources

Single Particle Adsorption and Response Quantification for Functional AAVx Titer and Dose Analysis

Accurate quantification of functional adeno-associated virus (AAV) dose remains a critical limitation in gene therapy, where titers are defined using ensemble measurements of viral genomes or capsid concentration that average across heterogeneous populations and weakly predict transduction. We present single-particle adsorption and response quantification (SPARQ), a diffraction-limited imaging platform for quantifying AAVx vectors, regardless of serotype, at single-nanoparticle and single-cell resolution. SPARQ immobilizes and resolves individual AAVx, enabling concurrent measurement of capsid-associated and genome-associated signals before cell exposure. Across multiple serotypes, including AAV2, AAV5, and AAVrh74, SPARQ identifies full-capsid fractions, consistent with bulk measurements obtained by ddPCR/ELISA, DLS/UV-Vis, charge detection, and mass photometry, while reporting narrower distributions than ensemble-derived values and revealing systematic discrepancies in bulk-derived titers arising from population averaging. Surface immobilization is achieved by charge-dependent AAVx-surface interactions, as supported by multiphysics simulations, which capture serotype-dependent adsorption kinetics governed by capsid electrostatics for AAV2, AAV5, AAV6, and AAV9. Furthermore, SPARQ directly measures transduction as a function of particle number and reveals a threshold response. Transduction efficiency increased from [~]29% (S.D {+/-} 3.31%) at [~]18 (S.D {+/-} 7.55) AAVs per cell to [~]66% (S.D {+/-} 1.66%) at [~]42 (S.D {+/-} 9.69) AAVs per cell, which is comparable with conventional in vitro assay requiring 105 AAVs/cell. Cumulative fluorescence measurements across large micro-patterned arrays of single cells recapitulate bulk-like high-throughput scaling, while SPARQs single-nanoparticle resolution reveals functional heterogeneity that is masked by population averaged assays. SPARQ provides a particle-resolved framework for functional AAVx titration and quantitative characterization, enabling the development of quality control and dosing strategies in gene therapy manufacturing. TeaserSPARQ combines light-activated surface viral adsorption with diffraction-limited imaging to directly quantify AAV integrity, heterogeneity, and functional transduction at the single-particle level.

bioengineering↗

LRP8 is a Receptor for Yellow Fever Virus

Yellow fever virus (YFV), an arbovirus causing substantial human morbidity and mortality, was the first human virus discovered over a century ago. The live-attenuated 17D vaccine is among the most successful vaccines in medicine. Despite the importance of YFV, its receptor has remained unknown. Here, we performed a barcoded, genome-wide human ORF library screen and identified LRP8 (also named APOER2) as a receptor for YFV. We show that LRP8 expression specifically boosts YFV infection in cell lines by promoting entry. AAV-mediated expression of human LRP8 in mouse liver aggravates infection and pathology. LRP8 knockdown abolishes YFV infection in brain cells, primary human hepatocytes, and notably in mosquitoes. Biochemically, LRP8 directly interacts with YFV particles via the viral envelope protein. This function of LRP8 is conserved across species, particularly in mosquitoes and primates. A soluble LRP8 decoy protein can block YFV infection in vitro and in mice, providing a potential therapeutic or prophylactic strategy. Our findings provide groundwork for understanding YFV entry, tropism, and pathogenesis, and may enable development of novel therapeutics to treat YFV infection.

microbiology↗