Hong Ka L, Battistella Luisa, Salva Alysia D, Williams Ryan M, Sooter Letha J
Department of Pharmaceutical Sciences, West Virginia University, 1 Medical Center Drive, P.O. Box 9530, Morgantown, WV 26506, USA.
Int J Mol Sci. 2015 Jan 27;16(2):2794-809. doi: 10.3390/ijms16022794.
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.
α毒素是金黄色葡萄球菌分泌的主要毒力因子之一,金黄色葡萄球菌可在社区和医院环境中引发多种感染。由于金黄色葡萄球菌相关感染的普遍性以及耐甲氧西林金黄色葡萄球菌的出现,快速准确地诊断金黄色葡萄球菌感染对于改善患者健康状况至关重要。在本研究中,我们利用实验室先前开发的一种严格的指数富集配体系统进化(SELEX)变体,筛选出一种对α毒素具有高亲和力和特异性的单链DNA分子识别元件(MRE)。在12轮筛选结束时,所选MRE的平衡解离常数(Kd)为93.7±7.0 nM。此外,通过使用所选的单链DNA MRE作为毒素捕获元件,开发了一种改良的夹心酶联免疫吸附测定(ELISA),并在未稀释的人血清样本中实现了对200 nMα毒素的灵敏检测。