4.7 Article

Target Affinity and Structural Analysis for a Selection of Norovirus Aptamers

Journal

Publisher

MDPI
DOI: 10.3390/ijms22168868

Keywords

aptamers; systematic evolution of ligands by exponential enrichment (SELEX); affinity; norovirus; virus like particles (VLPs)

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This study characterized seven previously described norovirus aptamers for their target affinity, structure, and potential applications. Four aptamers showed affinity for GII.4 strains, while three also exhibited affinity toward GII.3 and GI.7. Circular dichroism analysis revealed that most aptamers exhibited a B-DNA structure, with one displaying a G-quadruplex hybrid structure. These findings provide a knowledge base for future norovirus detection and extraction assay development using aptamer technology.
Aptamers, single-stranded oligonucleotides that specifically bind a molecule with high affinity, are used as ligands in analytical and therapeutic applications. For the foodborne pathogen norovirus, multiple aptamers exist but have not been thoroughly characterized. Consequently, there is little research on aptamer-mediated assay development. This study characterized seven previously described norovirus aptamers for target affinity, structure, and potential use in extraction and detection assays. Norovirus-aptamer affinities were determined by filter retention assays using norovirus genotype (G) I.1, GI.7, GII.3, GII.4 New Orleans and GII.4 Sydney virus-like particles. Of the seven aptamers characterized, equilibrium dissociation constants for GI.7, GII.3, GII.4 New Orleans and GII.4 Sydney ranged from 71 +/- 38 to 1777 +/- 1021 nM. Four aptamers exhibited affinity to norovirus GII.4 strains; three aptamers additionally exhibited affinity toward GII.3 and GI.7. Aptamer affinity towards GI.1 was not observed. Aptamer structure analysis by circular dichroism (CD) spectroscopy showed that six aptamers exhibit B-DNA structure, and one aptamer displays parallel/antiparallel G-quadruplex hybrid structure. CD studies also showed that biotinylated aptamer structures were unchanged from non-biotinylated aptamers. Finally, norovirus aptamer assay feasibility was demonstrated in dot-blot and pull-down assays. This characterization of existing aptamers provides a knowledge base for future aptamer-based norovirus detection and extraction assay development and aptamer modification.

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