Rapid and homogeneous electrochemical detection by fabricating a high affinity bispecific antibody-enzyme complex using two Catcher/Tag systems

被引:15
作者
Kimura, Hayato [1 ]
Miura, Daimei [1 ]
Tsugawa, Wakako [1 ]
Ikebukuro, Kazunori [1 ]
Sode, Koji [2 ,3 ]
Asano, Ryutaro [1 ]
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Biotechnol & Life Sci, Tokyo 1848588, Japan
[2] Univ N Carolina, Joint Dept Biomed Engn, Chapel Hill, NC USA
[3] North Carolina State Univ, Chapel Hill, NC 27599 USA
基金
日本学术振兴会;
关键词
Bispecific antibody-enzyme complex; Catcher/Tag system; Epidermal growth factor receptor; Glucose dehydrogenase; Homogeneous electrochemical detection; Single-chain Fv; PROTEIN; BIOSENSOR; DEHYDROGENASE; IMMUNOASSAY; SERUM;
D O I
10.1016/j.bios.2020.112885
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Antibody-enzyme complexes (AECs) with binding ability to specific targets and catalytic activities to gain signals are known to be ideal sensing elements; however, AEC-based universal sensors applicable to point-of-care testing (POCT) have not yet been developed. Here, we achieved rapid and homogeneous electrochemical detection by fabricating a high-affinity bispecific AEC (bsAEC) using two Catcher/Tag systems. Recently, we reported a convenient and universal method to fabricate AECs using the SpyCatcher/SpyTag system. The resultant anti-epidermal growth factor receptor (anti-EGFR) AEC worked efficiently as a sensing element; however, the sensitivities did not meet the clinically required detection range of the soluble ectodomain of EGFR (sEGFR). To induce high affinity even to monomeric targets like sEGFR, we designed a convenient fabrication method for bsAEC using two Catcher/Tag systems, which did not express cross-reactivity. The anti-EGFR bsAEC was successfully prepared by constructing glucose dehydrogenase with two different catcher domains at the N- and C-terminus and by combining two corresponding Tag-fused anti-EGFR single-chain Fvs (scFvs), which recognize different epitopes on sEGFR. As expected, bsAEC showed a higher affinity than that of bivalent AEC with two identical anti-EGFR scFvs at low concentrations of sEGFR, and met the clinically required detection range of sEGFR. Further, by combining magnet beads, we established a rapid and wash-free homogeneous electrochemical detection method. This study offers new insights into the fabrication of universal POCT devices.
引用
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页数:9
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