Department of Chemistry and Biochemistry and Center for Nanoscience, University of Missouri-St. Louis, St. Louis, MO 63121, USA.
Anal Biochem. 2012 Apr 1;423(1):178-83. doi: 10.1016/j.ab.2012.01.017. Epub 2012 Jan 28.
Polyamides (PAs) are distamycin-type ligands of DNA that bind the minor groove and are capable of sequence selective recognition. This capability provides a viable route to their development as therapeutics. Presented here is a simple and convenient fluorescence assay for PA-DNA binding. PAs are titrated into a sample of a hairpin DNA featuring a TAMRA dye attached to an internal dU near the PA binding site. In a study of 6 PAs, PA binding leads to a steady reproducible decrease in fluorescence intensity that can be used to generate binding isotherms. The assay works equally well with both short (6- to 8-ring) and long (14-ring) PAs, and K(d) values ranging from approximately 1 nM to at least 140 nM were readily obtained using a simple monochromator or filter configuration. Competition assays provide a means to assessing possible dye interference, which can be negligible. The assay can also be used to determine PA extinction coefficients and to measure binding kinetics; thus, it is an accessible and versatile tool for the study of PA properties and PA-DNA interactions.
聚酰胺(PAs)是 DNA 的道诺霉素型配体,可结合小沟并具有序列选择性识别能力。这种能力为将其开发为治疗药物提供了可行的途径。本文介绍了一种用于 PA-DNA 结合的简单方便的荧光测定法。将 PA 滴定到发夹 DNA 样品中,该 DNA 样品具有附着在 PA 结合位点附近内部 dU 的 TAMRA 染料。在对 6 种 PA 的研究中,PA 结合导致荧光强度稳定且可重复降低,可用于生成结合等温线。该测定法对短(6-8 环)和长(14 环)PA 均同样有效,并且使用简单的单色仪或滤光片配置可以轻松获得从约 1 nM 到至少 140 nM 的 Kd 值。竞争测定法提供了评估可能的染料干扰的方法,这种干扰可以忽略不计。该测定法还可用于确定 PA 消光系数和测量结合动力学;因此,它是研究 PA 性质和 PA-DNA 相互作用的一种易于使用且功能多样的工具。