Abstract
Objectives
Human heart-type fatty acid binding protein (HFABP) is a biomarker for diagnosis, risk assessment, and prognosis of acute myocardial infarction, and we aimed to establish an immunoassay for HFABP quantitation.
Methods
Human HFABP monoclonal antibodies (mAbs) were developed, evaluated by enzyme-linked immunosorbent assay, and a chemiluminescence enzyme immunoassay (CLEIA) generated. Analytical performance of the CLEIA was evaluated by measuring serum HFABP.
Results
The prokaryotically expressed rHFABP was purified and four anti-HFABP mAbs with superior detection performance were obtained after immunizing BALB/c mice. MAbs 2B8 and 6B3 were selected as respective capture and detection antibodies for HFABP measurement by CLEIA (detection range, 0.01–128 μg/L). Results using the CLEIA showed excellent correlation (r, 0.9622) and the correlation coefficient was 0.9809 (P < 0.05) by the Tukey test statistical analysis with those of latex-enhanced immunoturbidimetry in hospitals.
Conclusion
Our mAbs and CLEIA for HFABP detection represent new diagnostic tools for measurement of human serum HFABP.
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Funding
This work was supported by National Natural Science Foundation of China (No. 81702005), Hunan Provincial Natural Science Foundation of China (No. 2019JJ50370), Science and Technology Plan Project of Changsha (No. KQ1801039 and KQ1907130), Science and Technology Plan of Hunan Provincial People's Hospital (No. RS20160208), Scientific Research Project of Hunan Provincial Health Commission (B202311009257).
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RSL, JZ and YLQ designed the study. JZ, ZHZ, YW, QLW and RSL drafted and revised the manuscript. JZ, YX, XZ, and MFQ performed the research, collected data and analyzed the data. CX revised the manuscript. All the authors reviewed and approved the final manuscript.
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Zheng, J., Qiu, Y., Xu, Y. et al. Magnetic particle-based chemiluminescence immunoassay for serum human heart-type fatty acid binding protein measurement. Biotechnol Lett 45, 1431–1440 (2023). https://doi.org/10.1007/s10529-023-03425-4
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DOI: https://doi.org/10.1007/s10529-023-03425-4