Magnetic bead-gold nanoparticle hybrids probe based on optically countable gold nanoparticles with dark-field microscope for T4 polynucleotide kinase activity assay

被引:23
|
作者
Jin, Tian [1 ,2 ]
Zhang, Jiewen [1 ]
Zhao, Yuanfang [3 ]
Huang, Xiaoting [1 ,2 ]
Tan, Chunyan [1 ,2 ]
Sun, Shuqing [3 ,4 ]
Tan, Ying [1 ,2 ]
机构
[1] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, State Key Lab Chem Oncogenom, Key Lab Chem Biol, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Shenzhen Key Lab Minimal Invas Med Technol, Inst Opt Imaging & Sensing, Shenzhen 518055, Peoples R China
[4] Tsinghua Univ, Dept Biomed Engn, Beijing 100084, Peoples R China
关键词
T4 PNK activity; Dark field microscopy; Gold nanoparticles; Magnetic bead; LABEL-FREE DETECTION; LAMBDA EXONUCLEASE; STRAND DISPLACEMENT; DNA-REPAIR; BIOSENSOR; 3'-PHOSPHATASE; ENUMERATION; PLATFORM; TERMINI; LIGASE;
D O I
10.1016/j.bios.2019.111936
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
T4 polynucleotide kinase (T4 PNK) plays an essential role in DNA phosphorylation during the DNA repair process. Therefore, the sensitive, selective and convenient detection of T4 PNK activity is of great significance. In this work, we proposed a sensitive non-amplification strategy for the sensing of T4 PNK activity via dark field microscope (DFM) based on magnetic bead (MB)-gold nanoparticle (AuNP) hybrids probe, MB-dsDNA-AuNP (MDA). In the presence of T4 PNK, the 5'-OH termini of DNA are phosphorylated and cleaved into oligonucleotides by lambda exonuclease (lambda exo), resulting in the destruction of the MDA probe and the separation of AuNP from the MB. Through automatic counting of AuNPs from DFM images, T4 PNK activity can be quantitatively measured. This strategy revealed a limit of detection (LOD) as low as 0.0058 U/mL and exhibited a dynamic range from 0.01 to 1 U/mL. The strategy presents an excellent ability to discriminate T4 PNK from the other proteins and enzymes. Notably, this strategy was applied to screen the T4 PNK inhibitors and test the activity in cell lysates, showing great potential for the discovery of new anticancer drugs and other related research field.
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页数:7
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