The characterization and validation of 17β-estradiol binding aptamers. Issue 167 (March 2017)

• Record Type: Journal Article
• Authors: Svobodová, Markéta; Skouridou, Vasso; Botero, Mary Luz; Jauset-Rubio, Miriam; Schubert, Thomas; Bashammakh, Abdulaziz S.; El-Shahawi, Mohammad S.; Alyoubi, Abdulrahman O.; O'Sullivan, Ciara K.
• Is Part Of: Journal of steroid biochemistry and molecular biology. Issue 167(2017)
• Page Start: 14
• Page End: 22
• Publication Date: 2017-03
• Subjects: 17β-estradiol -- Aptamers -- Small molecule -- Microscale thermophoresis (MST) -- Apta-PCR affinity assay (APAA) -- Surface Plasmon Resonance (SPR); Steroid hormones -- Periodicals; Biochemistry -- Periodicals; Hormones -- Periodicals; Molecular Biology -- Periodicals; Hormones stéroïdes -- Périodiques; Steroid hormones; Periodicals; 572.579
• DOI: 10.1016/j.jsbmb.2016.09.018
• Languages: English
• ISSNs: 0960-0760

Abstract

Highlights: 17β-Estradiol aptamers were validated with three different techniques. Microscale Thermophoresis is suitable for monitoring aptamer-small molecule interactions. Aptamer-PCR affinity assay and Surface Plasmon Resonance can be used for screening of aptamers. Multiple methods are required for the evaluation of aptamer-small molecule interactions. Abstract: The rapid and sensitive detection of small molecules is garnering increasing importance, and aptamers show great promise in replacing expensive, elaborate detection platforms exploiting chromatographic separation or antibody-based assays. The characterization of aptamer interaction with small molecule targets is not facile, and there is a mature need for a rapid, high-throughput technique for the analysis of aptamer-small molecule kinetics and affinity. In this work we present methodologies for the evaluation of aptamer-small molecule interactions, using the aptamers reported against the steroid 17β-estradiol as a model system. Microscale thermophoresis, apta-PCR affinity assay and surface plasmon resonance were explored to evaluate the reported aptamers' binding properties in terms of affinity and specificity, and were demonstrated to be successfully applied to the analysis of aptamer-small molecule interactions.