Immunoassays/Immunosensors Laboratory Institute of Nuclear & Radiological Sciences & Technology, Energy & Safety, NCSR "Demokritos", 15341 Aghia Paraskevi, Greece.
Department of Chemistry, National and Kapodistrian University of Athens, University Campus, 15771 Athens, Greece.
Biosensors (Basel). 2024 Oct 6;14(10):479. doi: 10.3390/bios14100479.
Survivin belongs to a family of proteins that promote cellular proliferation and inhibit cellular apoptosis. Its overexpression in various cancer types has led to its recognition as an important marker for cancer diagnosis and treatment. In this work, we compare two approaches for the immunochemical detection of survivin through surface-enhanced fluorescence or Raman spectroscopy using surfaces with nanowires decorated with silver nanoparticles in the form of dendrites or aggregates as immunoassays substrates. In both substrates, a two-step non-competitive immunoassay was developed using a pair of specific monoclonal antibodies, one for detection and the other for capture. The detection antibody was biotinylated and combined with streptavidin labeled with rhodamine for the detection of surface-enhanced fluorescence, while, for the detection via Raman spectroscopy, streptavidin labeled with peroxidase was used and the signal was obtained after the application of 3,3',5,5'-tetramethylbenzidine (TMB) precipitating substrate. It was found that the substrate with the silver dendrites provided higher fluorescence signal intensity compared to the substrate with the silver aggregates, while the opposite was observed for the Raman signal. Thus, the best substrate was used for each detection method. A detection limit of 12.5 pg/mL was achieved with both detection approaches along with a linear dynamic range up to 500 pg/mL, enabling survivin determination in human serum samples from both healthy and ovarian cancer patients for cancer diagnosis and monitoring purposes.
Survivin 属于一类促进细胞增殖和抑制细胞凋亡的蛋白质家族。其在各种癌症类型中的过度表达使其成为癌症诊断和治疗的重要标志物。在这项工作中,我们比较了两种通过表面增强荧光或拉曼光谱法检测 survivin 的方法,使用纳米线表面作为免疫分析的基底,纳米线上的银纳米粒子呈树枝状或聚集态。在这两种基底中,均采用双抗体一步非竞争免疫法进行检测,一对特异性单克隆抗体,一种用于检测,另一种用于捕获。检测抗体被生物素化,与标记有罗丹明的链霉亲和素结合,用于检测表面增强荧光,而对于拉曼光谱检测,则使用标记有过氧化物酶的链霉亲和素,应用 3,3',5,5'-四甲基联苯胺(TMB)沉淀基底后获得信号。结果表明,与银聚集体基底相比,银树枝状基底提供了更高的荧光信号强度,而拉曼信号则相反。因此,针对每种检测方法,选择最佳的基底。两种检测方法的检测限均为 12.5 pg/mL,线性动态范围高达 500 pg/mL,可用于人血清样本中 survivin 的测定,以便进行癌症诊断和监测。