Selection of specific inhibitor peptides in enzyme-linked immunosorbent assay (ELISA) of cardiac troponin I using immuno-dominant epitopes as competitor

M. Rezaee, M. Rasaee, J. Mohammadnejad
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引用次数: 15

Abstract

ABSTRACT Human cardiac troponin I (cTni) is the gold marker for early diagnosis of myocardial infarction. In this regard, four immune-dominant epitopes of cTni were predicted and their 3D structures were determined. Thereafter, the competitive performance of the peptides was monitored with the developed polyclonal antibody-based indirect competitive ELISA; a half-maximal inhibitory concentration (IC50) of 0.49 (µg/mL) and detection limit of 0.037 (µg/mL) were achieved for recombinant cTni. The competitive ELISA determined sensitivity levels of 0.306, 0.141, 0.960, and 0.155 (µg/mL), respectively, for each peptide as competitor. We indicated that two of the selected epitopes have significant sensitivity scales and inhibition ability.
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以免疫显性表位为竞争对手的心肌肌钙蛋白I酶联免疫吸附试验(ELISA)中特异性抑制肽的选择
人心肌肌钙蛋白I (cTni)是心肌梗死早期诊断的金标记物。因此,我们预测了cTni的4个免疫显性表位,并确定了它们的三维结构。随后,利用建立的基于多克隆抗体的间接竞争ELISA检测肽段的竞争性能;重组cTni的半数最大抑制浓度(IC50)为0.49(µg/mL),检出限为0.037(µg/mL)。竞争酶联免疫吸附试验对竞争肽的敏感性分别为0.306、0.141、0.960和0.155(µg/mL)。我们发现两个选择的表位具有显著的敏感性尺度和抑制能力。
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