Document Type
Article
Publication Date
2015
College/Unit
School of Pharmacy
Department/Program/Center
Pharmaceutical Sciences
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.
Digital Commons Citation
Hong, Ka L.; Battistella, Luisa; Salva, Alysia D.; Williams, Ryan M.; and Sooter, Letha J., "In Vitro Selection of Single-Stranded DNA Molecular Recognition Elements against S. aureus Alpha Toxin and Sensitive Detection in Human Serum" (2015). Faculty & Staff Scholarship. 2311.
https://researchrepository.wvu.edu/faculty_publications/2311
Source Citation
Hong, K., Battistella, L., Salva, A., Williams, R., & Sooter, L. (2015). In Vitro Selection of Single-Stranded DNA Molecular Recognition Elements against S. aureus Alpha Toxin and Sensitive Detection in Human Serum. International Journal of Molecular Sciences, 16(2), 2794–2809. https://doi.org/10.3390/ijms16022794
Comments
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited