CNRS UMR9187, INSERM U1196, Institut Curie, PSL Research University, 91405, Orsay, France.
CNRS UMR9187, INSERM U1196, Université Paris Sud, Université Paris Saclay, 91405, Orsay, France.
Chemistry. 2019 Feb 1;25(7):1812-1818. doi: 10.1002/chem.201805422. Epub 2019 Jan 2.
The high-throughput assessment of the secondary structures adopted by DNA oligonucleotides is currently hampered by the lack of suitable biophysical methods. Fluorescent sensors hold great potential in this respect; however, the moderate selectivity that they display for one DNA conformation over the others constitutes a major drawback to the development of accurate assays. Moreover, the use of single sensors impedes a comprehensive classification of the tested sequences. Herein, we propose to overcome these limitations through the development of a fluorescence sensor array constituted by easily accessible, commercial dyes. Multivariate analysis of the emission data matrix produced by the array allows the conformational preferences of DNA sequences of interest to be explored, either by calculating the probability of group membership in the six predefined structural categories (three G-quadruplex groups, double-stranded, and two groups of single-stranded forms) or by revealing their particular structural features. The assay enables rapid screening of synthetic DNA oligonucleotides in a 96-well plate format.
目前,高通量评估 DNA 寡核苷酸所采用的二级结构受到缺乏合适的生物物理方法的限制。荧光传感器在这方面具有很大的潜力;然而,它们对一种 DNA 构象相对于其他构象的中等选择性是开发准确测定法的一个主要缺点。此外,单一传感器的使用妨碍了对所测试序列的全面分类。在此,我们建议通过开发由易于获得的商业染料组成的荧光传感器阵列来克服这些限制。通过对由该阵列产生的发射数据矩阵进行多元分析,可以探索感兴趣的 DNA 序列的构象偏好,既可以通过计算在六个预定义结构类别(三个 G-四链体组、双链和两组单链形式)中的组归属概率,也可以通过揭示它们的特殊结构特征来实现。该测定法能够以 96 孔板格式快速筛选合成 DNA 寡核苷酸。