Development of an Affimer-antibody combined immunological diagnosis kit for glypican-3

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作者
Chunmei Xie
Christian Tiede
Xuanyi Zhang
Congrong Wang
Zhixiong Li
Xiao Xu
Michael J. McPherson
Darren C. Tomlinson
Weiwen Xu
机构
[1] Southern Medical University,State Key Laboratory of Organ Failure Research, Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology
[2] Faculty of Biological Sciences,BioScreening Technology Group, School of Molecular and Cellular, Biology
[3] University of Leeds,Astbury Centre for Structural Molecular Biology
[4] Faculty of Biological Sciences,Department of Laboratory Medicine, Nanfang Hospital
[5] University of Leeds,undefined
[6] First Affiliated Hospital of Zhejiang University,undefined
[7] Southern Medical University,undefined
[8] R&D center,undefined
[9] DaRui Biotechnology Co.,undefined
[10] Ltd,undefined
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Scientific Reports | / 7卷
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摘要
Glypican-3 (GPC3) is a promising new marker for hepatocellular carcinoma, but the reported values for serum GPC3 differ markedly between currently available kits. Here we isolated Affimer non-antibody binding proteins against GPC3 by phage display and developed a new sandwich chemiluminescence immunoassay (CLIA) combining an Affimer with a monoclonal antibody (Affimer-MAb CLIA). The proposed CLIA assay demonstrated a wide linear range  0.03–600 ng/mL) with a good linear correlation coefficient (0.9999), a high detection limitation (0.03 ng/mL) and specificity (0–0.002%) for detection of GPC3. The accuracy, hook effect and stability were demonstrated to be satisfactory. The mean level of GPC3 in serum was higher (>8.5 fold, P < 0.001) in hepatocellular carcinoma patients compared to healthy and other liver disease individuals. A poor correlation (correlation coefficients ranged from −0.286 to 0.478) was observed through pairwise comparison within different kits. However, only this newly developed CLIA test showed high specificity and correlated with the “gold standard” GPC3-immunohistochemistry. This study indicates that Affimer-MAb CLIA can be used to generate a sensitive immunodiagnostic kit, which offers the potential for a highly specific clinically-relevant detection system.
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