Maity Debabrata, Matković Marija, Li Shang, Ehlers Martin, Wu Junchen, Piantanida Ivo, Schmuck Carsten
Institute of Organic Chemistry, University of Duisburg-Essen, 45117, Essen, Germany.
Ruđer Bošković Institute, HR-10000, Zagreb, Croatia.
Chemistry. 2017 Dec 6;23(68):17356-17362. doi: 10.1002/chem.201703813. Epub 2017 Nov 9.
This work reports two new peptide-based fluorescence probes (1 and 2) for the detection of ds-DNA at physiological pH. Probes 1 and 2 contain a fluorophore, either amino-naphthalimide or diethyl-aminocoumarin, respectively, and two identical peptide arms each equipped with a guanidiniocarbonylpyrrole (GCP) anion-binding motif. These probes show "switch-on" fluorescence response upon binding to ds-DNA, whereby they can differentiate between various types of polynucleotides. For instance, they exhibit more pronounced fluorescence response for AT-rich polynucleotides than GC-rich polynucleotides, and both give only negligible response to ds-RNA. The fluorimetric response of 1 is proportional to the AT-basepair content in DNA, whereas the fluorescence of 2 is sensitive to the secondary structure of the polynucleotide. Fluorescence experiments, thermal melting experiments and circular dichroism studies suggest that 1 interacts with ds-DNA in a combined intercalation and minor groove binding, whereas 2 interacts mainly with the outer surface of DNA/RNA. As 1 and 2 have a very low cytotoxicity, 1 can be applied for the imaging of nuclear DNA in cells.
这项工作报道了两种新型基于肽的荧光探针(1和2),用于在生理pH值下检测双链DNA。探针1和2分别含有一个荧光团,即氨基萘二甲酰亚胺或二乙氨基香豆素,以及两个相同的肽臂,每个肽臂都配备有胍基羰基吡咯(GCP)阴离子结合基序。这些探针在与双链DNA结合时表现出“开启”荧光响应,从而能够区分不同类型的多核苷酸。例如,它们对富含AT的多核苷酸表现出比富含GC的多核苷酸更明显的荧光响应,并且对双链RNA的响应都可以忽略不计。探针1的荧光响应与DNA中AT碱基对的含量成正比,而探针2的荧光对多核苷酸的二级结构敏感。荧光实验、热熔实验和圆二色性研究表明,探针1与双链DNA的相互作用是插入和小沟结合的组合方式,而探针2主要与DNA/RNA的外表面相互作用。由于探针1和2具有非常低的细胞毒性,探针1可用于细胞中核DNA的成像。