Research Center for Analytical Sciences, Department of Chemistry, College of Sciences, Northeastern University, Box 332, Shenyang, 110819, Liaoning, China.
College of Life and Health Sciences, Northeastern University, Shenyang, 110169, Liaoning, China.
Anal Bioanal Chem. 2021 Jul;413(17):4451-4458. doi: 10.1007/s00216-021-03399-0. Epub 2021 May 17.
Robust and sensitive cell-based enzyme-linked immunosorbent assay (CELISA) is of great significance in the diagnosis and screening of cancer. However, the method is limited by the high rate of negative results attributed to the instability of horseradish peroxidase (HRP), HO, and antibody. Here, we construct a folic acid-functionalized in situ-grown MnO nanosheet/graphene oxide hybrid (FA-MnO/GO) with oxidase-like activity instead of the anti-folate receptor antibody in traditional CELISA to resist the possible negative interference arising from unstable HRP, HO, and antibodies for more robust colorimetric detection of cancer cells. The functionalization of FA enables the selective binding between hybrid and cancer cells through the over-expressed folate receptor, and then the binding events are converted into quantitative colorimetric signals though the oxidation of the chromogenic substrate TMB catalyzed by MnO, allowing the detection of cancer cells with colorimetric method. Moreover, the construction of MnO/GO hybrid can synergistically enhance the oxidase-like activity of MnO and promote its dispersion in water, further ensuring the accuracy and sensitivity of the detection. A detection limit of 20 cancer cells is obtained by a plate reader, which is lower than those obtained by most reported CELISA methods for cancer cell detection, and as few as 75 cancer cells can be identified by the naked eye. This study not only provides a multifunctional sensing platform for robust and sensitive cancer cell detection, but also offers a promising oxidase-like mimic in the field of bioanalysis.
基于细胞的酶联免疫吸附测定(CELISA)具有稳健和灵敏的特点,在癌症的诊断和筛查中具有重要意义。然而,该方法受到辣根过氧化物酶(HRP)、HO 和抗体不稳定导致高阴性率的限制。在这里,我们构建了一种具有氧化酶样活性的叶酸功能化原位生长的 MnO 纳米片/氧化石墨烯杂化材料(FA-MnO/GO),以取代传统 CELISA 中的抗叶酸受体抗体,从而抵抗可能由于 HRP、HO 和抗体不稳定而产生的负干扰,实现对癌细胞的更稳健的比色检测。FA 的功能化使得杂化材料能够通过过表达的叶酸受体与癌细胞选择性结合,然后通过 MnO 催化显色底物 TMB 的氧化将结合事件转化为定量比色信号,从而通过比色法检测癌细胞。此外,MnO/GO 杂化的构建可以协同增强 MnO 的氧化酶样活性,并促进其在水中的分散,进一步确保检测的准确性和灵敏度。通过平板读数仪获得的检测限为 20 个癌细胞,低于大多数报道的用于癌细胞检测的 CELISA 方法的检测限,并且通过肉眼可以识别低至 75 个癌细胞。这项研究不仅为稳健和灵敏的癌细胞检测提供了一种多功能传感平台,而且为生物分析领域提供了一种有前途的氧化酶样模拟物。