Paul Ruma, Morales-Lozada Yermary, Sánchez Colón Brian J, Hernandez Andrea R, Roy Sourav, Cabrera Carlos R
Department of Chemistry and Biochemistry, The University of Texas at El Paso, El Paso, Texas 79968, United States.
Department of Chemistry, University of Puerto Rico, Río Piedras Campus, San Juan 00925-2537, Puerto Rico.
ACS Meas Sci Au. 2025 Feb 5;5(1):87-95. doi: 10.1021/acsmeasuresciau.4c00073. eCollection 2025 Feb 19.
Colorectal cancer (CRC) is one of the most treatable cancers, yet it ranks second in mortality worldwide. Early detection significantly impacts treatment outcomes, but early stage CRC often presents no symptoms or nonspecific symptoms. The current screening methods are invasive and lacks specificity, hindering widespread CRC screening efforts. This underscores the urgent need for improved CRC screening tools. In this study, a label-free impedimetric immunosensor for detecting colon cancer-secreted protein-2 (CCSP-2), which exhibits a mean 78-fold increase in primary colon cancers compared to normal mucosa, was developed. Our cost-effective and noninvasive electrochemical immunosensor for CCSP-2 biomarker detection aims to facilitate early diagnosis and monitoring of CRC. The designed immunosensor features a functionalized gold electrode (Au) modified with cysteine-modified recombinant protein G (RPGCys) to immobilize the CCSP-2 antibody (Ab), and bovine serum albumin (BSA) used to prevent sensor surface fouling. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) were employed to analyze the electrochemical response to the binding of CCSP-2 antigen (Ag) and Ab. The changes in relative charge transfer resistance (Δ / ) with varying concentrations of Ag were plotted and a calibration curve was established between Δ / and logarithm of Ag concentration to assess sensor's sensitivity. The sensor demonstrated a linear response ( = 0.95) within the range of 10-100 ng/μL, plateauing after 100 ng/μL, with a detection limit of 0.71 ng/μL. Statistical analysis of specificity and selectivity studies showed significant differences in Ag detection compared to blank and nonspecific protein BSA, both with and without cell extracts. This immunosensor effectively detects the CRC biomarker CCSP-2 with high sensitivity and specificity. Integrating this sensor with other sensors for serum CRC biomarkers present a promising approach for developing diagnostic and prognostic tools for CRC.
结直肠癌(CRC)是最可治疗的癌症之一,但在全球死亡率中排名第二。早期检测对治疗结果有重大影响,但早期结直肠癌通常没有症状或症状不具特异性。目前的筛查方法具有侵入性且缺乏特异性,阻碍了结直肠癌广泛筛查工作。这凸显了改进结直肠癌筛查工具的迫切需求。在本研究中,开发了一种用于检测结肠癌分泌蛋白-2(CCSP-2)的无标记阻抗免疫传感器,与正常黏膜相比,该蛋白在原发性结肠癌中平均增加了78倍。我们用于CCSP-2生物标志物检测的具有成本效益且非侵入性的电化学免疫传感器旨在促进结直肠癌的早期诊断和监测。所设计的免疫传感器具有用半胱氨酸修饰的重组蛋白G(RPGCys)功能化的金电极(Au)以固定CCSP-2抗体(Ab),并使用牛血清白蛋白(BSA)防止传感器表面污染。采用电化学阻抗谱(EIS)和循环伏安法(CV)分析对CCSP-2抗原(Ag)与Ab结合的电化学响应。绘制了不同浓度Ag下相对电荷转移电阻(Δ / )的变化,并建立了Δ / 与Ag浓度对数之间的校准曲线以评估传感器的灵敏度。该传感器在10 - 100 ng/μL范围内表现出线性响应( = 0.95),在100 ng/μL后趋于平稳,检测限为0.71 ng/μL。特异性和选择性研究的统计分析表明,与空白和非特异性蛋白BSA相比,无论有无细胞提取物,在Ag检测方面都有显著差异。这种免疫传感器能以高灵敏度和特异性有效检测结直肠癌生物标志物CCSP-2。将该传感器与用于血清结直肠癌生物标志物的其他传感器整合,为开发结直肠癌诊断和预后工具提供了一种有前景的方法。