详细信息

A colorimetric aptasensor based on a hemin/EpCAM aptamer DNAzyme for sensitive exosome detection  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:A colorimetric aptasensor based on a hemin/EpCAM aptamer DNAzyme for sensitive exosome detection

作者:Kuang, Jingjing[1];Fu, Zhibo[1];Sun, Xuezhi[1];Lin, Chuhui[1];Yang, Shenglong[1];Xu, Jiayao[1];Zhang, Min[2];Zhang, Hongyang[1];Ning, Fanghong[3];Hu, Ping[1]

机构:[1]East China Univ Sci & Technol, Sch Chem Mol Engn, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Pharm, Minist Educ, Engn Res Ctr Pharmaceut Proc Chem, Shanghai 200237, Peoples R China;[3]East China Univ Sci & Technol, Sch Biotechnol, Shanghai 200237, Peoples R China

年份:2022

卷号:147

期号:22

起止页码:5054

外文期刊名:ANALYST

收录:;EI(收录号:20224413044819);WOS:【SCI-EXPANDED(收录号:WOS:000863908200001)】;

基金:This work was supported by the National Natural Science Foundation of China (Grant number 81973285).

语种:英文

外文关键词:Colorimetry - Diseases - Dissociation - Mammals - Proteins

摘要:Exosomes are considered as potential biomarkers that can reflect information from their parent cell-associated cancer microenvironment. Recently, aptasensors have been widely used for cancer and tumor exosome detection. Aptamers related to exosome surface proteins are usually used to introduce a sequence; the aptamer is used for exosome recognition, and the introduced sequence is used to form G-quadruplexes and for signal amplification. In this paper, we found that the EpCAM aptamer is rich in guanine and unimolecular G-quadruplex with a two-layer G-tetrad under acidic conditions, and we investigated its topology, thermal stability and dissociation constant with hemin. Based on this, our proposed colorimetric aptamer sensor combines the unmodified EpCAM aptamer with hemin to construct a hemin/G-quadruplex DNAzyme and catalyze the TMB-H2O2 system to generate a strong colorimetric signal. Therefore, colorimetric signal changes were negatively correlated with the exosome concentration. The linear range of the 1 h assay was 10(6)-10(8) particles per mL, and the detection limit was 3.94 x 10(5) particles per mL. In addition, this method can detect exosomes in complex fetal bovine serum samples with good specificity and high sensitivity toward exosomes from breast, liver, and lung cancers with abnormal EpCAM protein expression.

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