Peterson Amberlyn M, Jahnke Frank M, Heemstra Jennifer M
Department of Chemistry and the Center for Cell and Genome Science, University of Utah , Salt Lake City, Utah 84112, United States.
Sonata Biosciences, Inc., Auburn, California 95603, United States.
Langmuir. 2015 Nov 3;31(43):11769-73. doi: 10.1021/acs.langmuir.5b02818. Epub 2015 Oct 21.
Nucleic acid aptamers have a number of advantages compared to antibodies, including greater ease of production and increased thermal stability. We hypothesized that aptamers may also be capable of functioning in the presence of high concentrations of surfactants, which readily denature antibodies and other protein-based affinity reagents. Here we report the first systematic investigation into the compatibility of DNA aptamers with surfactants. We find that neutral and anionic surfactants have only a minor impact on the ability of aptamers to fold and bind hydrophilic target molecules. Additionally, we demonstrate that surfactants can be utilized to modulate the substrate binding preferences of aptamers, likely due to the sequestration of hydrophobic target molecules within micelles. The compatibility of aptamers with commonly used surfactants is anticipated to expand their scope of potential applications, and the ability to modulate the substrate binding preferences of aptamers using a simple additive provides a novel route to increasing their selectivity in analytical applications.
与抗体相比,核酸适配体具有许多优势,包括生产更简便以及热稳定性更高。我们推测,适配体在高浓度表面活性剂存在的情况下也可能发挥作用,而表面活性剂很容易使抗体和其他基于蛋白质的亲和试剂变性。在此,我们报告了对DNA适配体与表面活性剂兼容性的首次系统性研究。我们发现,中性和阴离子表面活性剂对适配体折叠及结合亲水性靶分子的能力仅有轻微影响。此外,我们证明表面活性剂可用于调节适配体的底物结合偏好,这可能是由于胶束内疏水性靶分子的隔离所致。适配体与常用表面活性剂的兼容性有望扩大其潜在应用范围,并且利用一种简单添加剂调节适配体底物结合偏好的能力为提高其在分析应用中的选择性提供了一条新途径。