Harkai Ákos, Beck Yoon Kee, Tory Anna, Mészáros Tamás
Department of Molecular Biology, Institute of Biochemistry and Molecular Biology, Semmelweis University, Tűzoltó street 37-47., 1094 Budapest, Hungary.
Department of Molecular Biology, Institute of Biochemistry and Molecular Biology, Semmelweis University, Tűzoltó street 37-47., 1094 Budapest, Hungary.
Int J Biol Macromol. 2025 Feb;288:138579. doi: 10.1016/j.ijbiomac.2024.138579. Epub 2024 Dec 8.
Streptococcus mutans is a commensal oral bacterium, yet its capacity for extensive biofilm formation is a major contributor to dental caries. This study presents a novel biofilm inhibition strategy by targeting GbpC, a cornerstone protein in S. mutans biofilm architecture, with specific DNA aptamers. Using SELEX (Systematic Evolution of Ligands by EXponential enrichment), we selectively targeted the extracellular domain of GbpC while incorporating structurally similar antigen I/II protein and a GbpC-deficient S. mutans strain as counter-targets to ensure high specificity. Aptamer selection was further refined through a panning method that combined primer-blocked asymmetric PCR with AlphaScreen technology. Detailed binding analyses via biolayer interferometry and microscale thermophoresis confirmed the interaction between top aptamer candidates and GbpC. Functional assays demonstrated that two lead aptamers evidently inhibited biofilm formation in wild-type S. mutans without affecting the GbpC-deficient strain, highlighting the aptamers' specificity. These results confirm that the selected aptamers retain specificity even in the complex bacterial culture matrix, validating the efficacy of our selection approach. Notably, these aptamers represent the first instance of using DNA aptamers to inhibit S. mutans biofilm formation by disrupting glucan binding. These aptamers hold promise as lead molecules for the development of biofilm-targeting therapies in dental care.
变形链球菌是一种口腔共生细菌,但其广泛形成生物膜的能力是导致龋齿的主要因素。本研究提出了一种新的生物膜抑制策略,即利用特异性DNA适配体靶向GbpC(变形链球菌生物膜结构中的关键蛋白)。通过指数富集配体系统进化技术(SELEX),我们在纳入结构相似的抗原I/II蛋白和GbpC缺陷型变形链球菌菌株作为反靶点以确保高特异性的同时,选择性地靶向GbpC的胞外结构域。通过将引物阻断不对称PCR与AlphaScreen技术相结合的淘选方法进一步优化适配体选择。通过生物层干涉术和微量热泳动进行的详细结合分析证实了顶级适配体候选物与GbpC之间的相互作用。功能测定表明,两种先导适配体明显抑制野生型变形链球菌中的生物膜形成,而不影响GbpC缺陷型菌株,突出了适配体的特异性。这些结果证实,即使在复杂的细菌培养基质中,所选适配体仍保持特异性,验证了我们选择方法的有效性。值得注意的是,这些适配体代表了通过破坏葡聚糖结合来使用DNA适配体抑制变形链球菌生物膜形成的首例。这些适配体有望成为牙科护理中生物膜靶向治疗开发的先导分子。