Cen Yao, Yang Yuan, Yu Ru-Qin, Chen Ting-Ting, Chu Xia
State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.
Nanoscale. 2016 Apr 21;8(15):8202-9. doi: 10.1039/c6nr01427e.
Phosphorylation of nucleic acids with 5'-OH termini catalyzed by polynucleotide kinase (PNK) is an inevitable process and has been implicated in many important cellular events. Here, we found for the first time that there was a significant difference in the adsorbent ability of cobalt oxyhydroxide (CoOOH) nanoflakes between single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA), which resulted in the fluorescent dye-labeled dsDNA still retaining strong fluorescence emission, while the fluorescence signal of ssDNA was significantly quenched by CoOOH nanoflakes. Based on this discovery, we developed a CoOOH nanoflake-based nanoprobe for the fluorescence sensing of T4 PNK activity and its inhibition by combining it with λ exonuclease cleavage reaction. In the presence of T4 PNK, dye-labeled dsDNA was phosphorylated and then cleaved by λ exonuclease to generate ssDNA, which could adsorb on the CoOOH nanoflakes and whose fluorescence was quenched by CoOOH nanoflakes. Due to the high quenching property of CoOOH nanoflakes as an efficient energy acceptor, a sensitive and selective sensing approach with satisfactory performance for T4 PNK sensing in a complex biological matrix has been successfully constructed and applied to the screening of inhibitors. The developed approach may potentially provide a new platform for further research, clinical diagnosis, and drug discovery of nucleotide kinase related diseases.
由多核苷酸激酶(PNK)催化的5'-OH末端核酸磷酸化是一个不可避免的过程,并且与许多重要的细胞事件有关。在这里,我们首次发现,氢氧化氧钴(CoOOH)纳米片对单链DNA(ssDNA)和双链DNA(dsDNA)的吸附能力存在显著差异,这导致荧光染料标记的dsDNA仍保留强烈的荧光发射,而ssDNA的荧光信号被CoOOH纳米片显著淬灭。基于这一发现,我们开发了一种基于CoOOH纳米片的纳米探针,通过将其与λ核酸外切酶切割反应相结合,用于荧光传感T4 PNK活性及其抑制作用。在T4 PNK存在的情况下,染料标记的dsDNA被磷酸化,然后被λ核酸外切酶切割生成ssDNA,ssDNA可吸附在CoOOH纳米片上,其荧光被CoOOH纳米片淬灭。由于CoOOH纳米片作为高效能量受体具有高淬灭特性,已成功构建了一种对复杂生物基质中的T4 PNK传感具有令人满意性能的灵敏且选择性的传感方法,并应用于抑制剂的筛选。所开发的方法可能为核苷酸激酶相关疾病的进一步研究、临床诊断和药物发现提供一个新的平台。