Dadakhani Sonya, Dehghan Gholamreza, Khataee Alireza
Department of Biology, Faculty of Natural Sciences, University of Tabriz, 51666-16471 Tabriz, Iran.
Department of Biology, Faculty of Natural Sciences, University of Tabriz, 51666-16471 Tabriz, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2023 Dec 5;302:123016. doi: 10.1016/j.saa.2023.123016. Epub 2023 Jun 17.
Many compounds such as amino acids and oligonucleotides have been shown to effectively change peroxidase-like activity of nanoparticles. While a few studies have focused on mimicking the active site of natural enzymes on nanozymes and thus increasing their substrate affinity. Therefore, in this work, the surface of FeCo@WO nanocomposite was modified using guanosine triphosphate (GTP) to mimic the histidine of peroxidase enzyme's active site and its modification was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier-transform infrared spectroscopy (FT-IR). Then, the peroxidase-mimicking activity of the modified nanocomposite was tested using a colorimetric method, based on the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (HO). It was found that GTP improves the activity of FeCo@WO as a natural peroxidase active site's distal histidine residue. Ascorbic acid (AA) is a powerful antioxidant that induces the reduction of blue color (oxidized TMB) ox-TMB to colorless TMB. The colorimetric method was applied for the sensitive detection of AA in common fruits. The linear range of AA was 10-100 μM with a limit of detection (LOD) of 0.27 μM, which provides a rapid and sensitive method for testing AA in the field of food analysis.
许多化合物,如氨基酸和寡核苷酸,已被证明能有效改变纳米颗粒的过氧化物酶样活性。虽然有一些研究专注于在纳米酶上模拟天然酶的活性位点,从而提高其对底物的亲和力。因此,在本工作中,使用鸟苷三磷酸(GTP)对FeCo@WO纳米复合材料的表面进行修饰,以模拟过氧化物酶活性位点的组氨酸,并通过X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和傅里叶变换红外光谱(FT-IR)对其修饰进行表征。然后,基于在过氧化氢(HO)存在下3,3',5,5'-四甲基联苯胺(TMB)的氧化反应,采用比色法测试修饰后纳米复合材料的过氧化物酶模拟活性。结果发现,GTP作为天然过氧化物酶活性位点的远端组氨酸残基,提高了FeCo@WO的活性。抗坏血酸(AA)是一种强大的抗氧化剂,能诱导蓝色(氧化型TMB)ox-TMB还原为无色的TMB。该比色法用于常见水果中AA的灵敏检测。AA的线性范围为10 - 100 μM,检测限(LOD)为0.27 μM,为食品分析领域中AA的检测提供了一种快速灵敏的方法。