Alemán Elvin A, de Silva Chamaree, Patrick Eric M, Musier-Forsyth Karin, Rueda David
Department of Chemistry, Wayne State University , 5101 Cass Avenue, Detroit, Michigan 48202, United States.
Department of Chemistry and Biochemistry, Center for RNA Biology, The Ohio State University , 100 West 18th Avenue, Columbus, Ohio 43210, United States.
J Phys Chem Lett. 2014 Mar 6;5(5):777-781. doi: 10.1021/jz4025832. Epub 2014 Feb 6.
Fluorescent nucleotide analogues, such as 2-aminopurine (2AP) and pyrrolo-C (PyC), have been extensively used to study nucleic acid local conformational dynamics in bulk experiments. Here we present a proof-of-principle approach using 2AP and PyC fluorescence at the single-molecule level. Our data show that ssDNA, dsDNA, or RNA containing both 2AP and PyC can be monitored using single-molecule fluorescence and a click chemistry immobilization method. We demonstrate that this approach can be used to monitor DNA and RNA in real time. This is the first reported assay using fluorescent nucleotide analogs at the single-molecule level. We anticipate that single 2AP or PyC fluorescence will have numerous applications in studies of DNA and RNA, including protein-induced base-flipping dynamics in protein-nucleic acid complexes.
荧光核苷酸类似物,如2-氨基嘌呤(2AP)和吡咯并-C(PyC),已被广泛用于在大量实验中研究核酸局部构象动力学。在此,我们展示了一种在单分子水平上使用2AP和PyC荧光的原理验证方法。我们的数据表明,含有2AP和PyC的单链DNA、双链DNA或RNA可以使用单分子荧光和点击化学固定方法进行监测。我们证明这种方法可用于实时监测DNA和RNA。这是首次报道的在单分子水平上使用荧光核苷酸类似物的检测方法。我们预计,单个2AP或PyC荧光在DNA和RNA研究中将有众多应用,包括蛋白质-核酸复合物中蛋白质诱导的碱基翻转动力学研究。