Quinone-based antibody labeling reagent for enzyme-free chemiluminescent immunoassays. Application to avidin and biotinylated anti-rabbit IgG labeling

被引:31
作者
El-Maghrabey, Mahmoud [1 ,2 ]
Kishikawa, Naoya [1 ]
Harada, Shiori [1 ]
Ohyama, Kaname [3 ]
Kuroda, Naotaka [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Course Pharmaceut Sci, Dept Analyt Chem Pharmaceut, 1-14 Bunkyo Machi, Nagasaki 8528521, Japan
[2] Mansoura Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Mansoura 35516, Egypt
[3] Nagasaki Univ, Grad Sch Biomed Sci, Dept Pharm Practice, 1-7-1 Sakamoto Machi, Nagasaki 8528588, Japan
基金
日本学术振兴会;
关键词
Non-enzymatic sensor; Biotin; Quinone; Chemiluminescence; Immunoassay; Stability; HORSERADISH-PEROXIDASE; PROTEIN ADDUCTS; NANOPARTICLES; MECHANISM; AZIDE;
D O I
10.1016/j.bios.2020.112215
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Chemiluminescence-enzyme immunoassays make it possible to measure trace components with high sensitivity and selectivity due to the high specificity of the antigen-antibody reaction and the high sensitivity of chemiluminescence assays. However, using an enzyme-labeled antibody suffers from many problems such as low reproducibility due to the instability of the enzyme and inhibition of antigen-antibody reaction due to its steric effect. Therefore, herein we report an innovative non-enzymatic chemiluminescence immunoassays labeling reagent through using quinone as a signal-generating tag coupled with biotin as a binder, to overcome enzymatic labeling problems. Biotinylated-1,4-naphthoquinone (biotin-NQ) was synthesized and characterized and it could produce long-lasting chemiluminescence upon mixing with dithiothreitol and luminol based on the redox cycle of quinone. Biotin-NQ showed exceptional stability towards different stress factors that may be encountered during performing the immunoassay such as high temperatures, highly acidic and alkaline conditions, and repeated freeze-thaw cycles. On the other hand, all these conditions lead to decreased labeling enzyme reactivity due to possible denaturation of its protein structure. Finally, the measurement of the biotin-labeled antibody was successfully performed using biotin-NQ and avidin. As a result, the antibody could be detected down to 25.7 nM which is 2.5 times sensitive than biotin-HRP chemiluminescence-enzyme immunoassays. Moreover, our method was applied successfully for determination of avidin using immobilized biotinylated antibody and biotin-NQ, which simulates immunoassays. Avidin could be detected down to 23.4 nM with excellent linearity (r = 0.996). Accordingly, our developed reagent, biotin-NQ, could be used as a universal highly stable, cost-effective, and steric free non-enzymatic label for immunoassays.
引用
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页数:9
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