Department of Chemistry, University of Oxford, South Parks Road, Oxford OX1 3QZ, U.K.
ACS Sens. 2024 Mar 22;9(3):1475-1481. doi: 10.1021/acssensors.3c02568. Epub 2024 Mar 5.
As a tumor-suppressing protein, p53 plays a crucial role in preventing cancer development. Its utility as an early cancer detection tool is significant, potentially enabling clinicians to forestall disease advancement and improve patient prognosis. In response to the pathological overexpression of this antigen in tumors, the prevalence of anti-p53 antibodies increases in serum, in a manner quantitatively indicative of cancer progression. This spike can be detected through techniques, such as Western blotting, immunohistochemistry, and immunoprecipitation. In this study, we present an electrochemical approach that supports ultrasensitive and highly selective anti-p53 autoantibody quantification without the use of an immuno-modified electrode. We specifically employ antigen-mimicking and antibody-capturing peptide-coated magnetic nanoparticles, along with an AC magnetic field-promoted sample mixing, prior to the presentation of Fab-captured targets to simple lectin-modified sensors. The subfemtomolar assays are highly selective and support quantification from serum-spiked samples within minutes.
作为一种肿瘤抑制蛋白,p53 在预防癌症发展方面起着至关重要的作用。它作为一种早期癌症检测工具的用途非常重要,有可能使临床医生能够阻止疾病的进展并改善患者的预后。针对肿瘤中这种抗原的病理性过表达,血清中抗 p53 抗体的流行率增加,以定量方式指示癌症的进展。这种峰值可以通过 Western blot、免疫组织化学和免疫沉淀等技术检测到。在这项研究中,我们提出了一种电化学方法,支持超灵敏和高度选择性的抗 p53 自身抗体定量,而无需使用免疫修饰电极。我们特别使用了模拟抗原和抗体捕获肽涂覆的磁性纳米颗粒,并在将 Fab 捕获的靶标呈现给简单的凝集素修饰传感器之前,使用交流磁场促进样品混合。亚飞摩尔检测具有高度选择性,并支持在数分钟内从血清加标样品中进行定量。