Mohammadi Somayeh, Salimi Abdollah, Hamd-Ghadareh Somayeh, Fathi Fardin, Soleimani Farzad
Department of Chemistry, University of Kurdistan, 66177-15175, Sanandaj, Iran.
Department of Chemistry, University of Kurdistan, 66177-15175, Sanandaj, Iran; Research Center for Nanotechnology, University of Kurdistan, 66177-15175, Sanandaj, Iran.
Anal Biochem. 2018 Sep 15;557:18-26. doi: 10.1016/j.ab.2018.06.008. Epub 2018 Jun 14.
We proposed a FRET immunosensing for detection of CA15-3 tumor marker by highly biospecific interactions between CA 15-3 antigen and the corresponding antibody and aptamer. In this sandwich type immunoassay, CA15-3 antibody-functionalized carbon dots and AuNPs labeled PAMAM-Dendrimer/aptamer were used as donor/acceptor, respectively. When CA 15-3 Ag was added to homogenous immunoassay, the strong complex interaction between CA15-3 Ab-CA15-3 Ag- aptamer caused in more coming closer carbon dot and AuNPs and more decreasing fluorescence signal. The decreased fluorescence intensity was linear at three ranges including in concentration range 1.1 μUmL to 16 μU mL with regression of R = 0.9879, at the concentration range 16 μU mL to 0.163 mU mL with regression of R = 0.9944 and at the concentration range 0.163 mU mL to 5.0 mU mL with regression of R = 0.9805. The detection limit of the FRET immunoassay was 0.9 μU mL. This assay revealed good sensitivity and specificity with MDA-MB-231 breast cancer cells concentrations from 1000 to 40000 cells/mL with correlation coefficient of 0.9955 and detection limit of 300 cells/mL (3 cells in 10 μL of injected sample). In addition, this FRET immunosensing is applicable in diluted human serum. The recovery values were in the range of 95.86-96.97% for CA 15-3 Ag in spiked serum sample with RSD lower than 7.3%. The proposed immunoassay could be a valid model for establishing other immunoassays for detection of different cancer tumor markers with relevant antigens and antibodies.
我们提出了一种荧光共振能量转移免疫传感方法,通过CA 15-3抗原与相应抗体和适配体之间的高度生物特异性相互作用来检测CA15-3肿瘤标志物。在这种夹心型免疫分析中,CA15-3抗体功能化的碳点和金纳米颗粒标记的聚酰胺-胺树枝状大分子/适配体分别用作供体/受体。当将CA 15-3抗原添加到均相免疫分析中时,CA15-3抗体-CA15-3抗原-适配体之间强烈的复合物相互作用导致碳点和金纳米颗粒靠得更近,荧光信号进一步降低。荧光强度的降低在三个浓度范围内呈线性关系,包括在1.1 μU/mL至16 μU/mL的浓度范围内,回归系数R = 0.9879;在16 μU/mL至0.163 mU/mL的浓度范围内,回归系数R = 0.9944;在0.163 mU/mL至5.0 mU/mL的浓度范围内,回归系数R = 0.9805。荧光共振能量转移免疫分析的检测限为0.9 μU/mL。该分析方法对MDA-MB-231乳腺癌细胞浓度在1000至40000个细胞/mL范围内显示出良好的灵敏度和特异性,相关系数为0.9955,检测限为300个细胞/mL(10 μL注射样品中有3个细胞)。此外,这种荧光共振能量转移免疫传感方法适用于稀释的人血清。在加标血清样品中,CA 15-3抗原的回收率在95.86 - 96.97%范围内,相对标准偏差低于7.3%。所提出的免疫分析方法可能是建立用于检测具有相关抗原和抗体的不同癌症肿瘤标志物的其他免疫分析方法的有效模型。