Electrochemical Strategy for Sensing Protein Phosphorylation

被引:79
作者
Miao, Peng [1 ,2 ,3 ]
Ning, Limin [2 ,3 ]
Li, Xiaoxi [2 ,3 ]
Li, Pengfei [1 ]
Li, Genxi [1 ,2 ,3 ]
机构
[1] Shanghai Univ, Sch Life Sci, Lab Biosensing Technol, Shanghai 200444, Peoples R China
[2] Nanjing Univ, Dept Biochem, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Natl Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
关键词
ROLLING-CIRCLE AMPLIFICATION; KINASE;
D O I
10.1021/bc200523p
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We herein report a novel electrochemical method in this paper to monitor protein phosphorylation and to assay protein kinase activity based on Zr4+ mediated signal transition and rolling circle amplification (RCA). First, substrate peptide immobilized on a gold electrode can be phosphorylated by protein kinase A. Then, Zr4+ links phosphorylated peptide and DNA primer probe by interacting with the phosphate groups. After the introduction of the padlock probe and phi29 DNA polymerase, RCA is achieved on the surface of the electrode. As the RCA product, a very long DNA strand, may absorb a large number of electrochemical speices, [Ru(NH3)(6)](3+), via the electrostatic interaction, localizing them onto the electrode surface, initiated by protein kinase A, a sensitive electrochemical method to assay the enzyme activity is proposed. The detection limit of the method is as low as 0.5 unit/mL, which might promise this method as a good candidate for monitoring phosphorylation in the future.
引用
收藏
页码:141 / 145
页数:5
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