Abstract
Alpha toxin is one of the major virulence factors secreted by Staphylococcus aureus, a bacterium that is responsible for a wide variety of infections in both community and hospital settings. Due to the prevalence of S. aureus related infections and the emergence of methicillin-resistant S. aureus, rapid and accurate diagnosis of S. aureus infections is crucial in benefiting patient health outcomes. In this study, a rigorous Systematic Evolution of Ligands by Exponential Enrichment (SELEX) variant previously developed by our laboratory was utilized to select a single-stranded DNA molecular recognition element (MRE) targeting alpha toxin with high affinity and specificity. At the end of the 12-round selection, the selected MRE had an equilibrium dissociation constant (Kd) of 93.7 ± 7.0 nM. Additionally, a modified sandwich enzyme-linked immunosorbent assay (ELISA) was developed by using the selected ssDNA MRE as the toxin-capturing element and a sensitive detection of 200 nM alpha toxin in undiluted human serum samples was achieved.
| Original language | English |
|---|---|
| Pages (from-to) | 2794-2809 |
| Number of pages | 16 |
| Journal | International Journal of Molecular Sciences |
| Volume | 16 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 27 2015 |
Keywords
- Alpha toxin
- Aptamer
- ELISA
- In vitro selection
- Molecular recognition element (MRE)
- SELEX
- SsDNA
- Staphylococcus aureus
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