化学
适体
检出限
寡核苷酸
DNA
抗体
毛细管电泳
色谱法
分子生物学
生物化学
免疫学
生物
作者
Masanobu Nagano,Takumi Toda,Kurumi Makino,Hiroko Miki,Yoshiaki Sugizaki,Hideyuki Tomizawa,Atsunobu Isobayashi,Keitaro Yoshimoto
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-11-30
卷期号:94 (49): 17255-17262
被引量:20
标识
DOI:10.1021/acs.analchem.2c04182
摘要
High-dose methotrexate (MTX) therapy is used to treat a wide variety of cancers such as leukemia and lymphoma, while the resulting high blood concentration of MTX faces a risk of life-threatening side effects, so it is essential to monitor the concentration carefully. Currently, the MTX concentration is measured using antibody-based kits in a clinical setting; however, the heterogeneity and batch-to-batch variation of antibodies potentially compromise the detection limit. Here, we developed MTX detection systems with chemically synthesizable homogeneous oligonucleotides. Microbead-assisted capillary electrophoresis (MACE)-SELEX against MTX successfully identified MSmt7 with a similar level of specificity to anti-MTX antibodies within three rounds. The 3'-end of MSmt7 was coupled to a peroxidase-like hemin-DNAzyme to construct a bifunctional oligonucleotide for MTX sensing, where MTX in 50% human serum was detected with a limit of detection (LoD) of 118 nM. Furthermore, amplifying the DNAzyme region with rolling circle amplification significantly improved the sensitivity with an LoD of 290 pM. Presented oligonucleotide-based MTX detection systems will pave the way for antibody-independent MTX detection with reliability and less cost in the laboratory and the clinic.
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