Ranjan Nihar, Arya Dev P
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER)-Raebareli, New Transit Campus, Lucknow, India.
Laboratory of Bioorganic and Medicinal Chemistry, Department of Chemistry, Clemson University, Clemson, SC, United States.
Methods Enzymol. 2019;623:291-314. doi: 10.1016/bs.mie.2019.05.027. Epub 2019 Jun 13.
RNA targeted high-throughput assays that allow for rapid detection of high affinity binding ligands are important in RNA recognition studies. A number for fluorescent dyes have been reported that can assist in rapidly identifying nucleic acid (RNA) binding elements without the need for immobilization of RNA or the ligand. A number of these dyes are planar aromatic molecules that bind non-specifically to nucleic acids and often distort their parent nucleic acid structures leading to ambiguity in the interpretation of results. In this light, we report here, the use of an aminoglycoside (neomycin) based fluorescent probe (F-Neo) which can reversibly bind to different RNA motifs and help identify ligands with needed affinity and selectivity, without any immobilization of the probe or the target. In this chapter, we provide the details of the assay development, experimental considerations and data analysis to use the probe and identify novel ligands. We then provide a brief introduction to calorimetry (ITC) and circular dichroism (CD) spectroscopy based methods in validating the binding of such identified compounds.
能够快速检测高亲和力结合配体的RNA靶向高通量检测方法在RNA识别研究中至关重要。已经报道了多种荧光染料,它们能够在无需固定RNA或配体的情况下,协助快速鉴定核酸(RNA)结合元件。其中许多染料是平面芳香分子,它们与核酸非特异性结合,并且常常扭曲其母核酸结构,导致结果解释存在歧义。有鉴于此,我们在此报告一种基于氨基糖苷(新霉素)的荧光探针(F-Neo)的应用,它能够与不同的RNA基序可逆结合,并有助于鉴定具有所需亲和力和选择性的配体,而无需固定探针或靶标。在本章中,我们详细介绍了该检测方法的开发、实验注意事项以及使用该探针鉴定新型配体的数据分析。然后,我们简要介绍基于量热法(ITC)和圆二色性(CD)光谱的方法,用于验证此类鉴定化合物的结合情况。