Liu Jing, Wang Tianze, Xiao Bo, Deng Muhan, Yu Peng, Qing Taiping
School of Materials Science and Engineering, Xiangtan University, Xiangtan 411105, PR China.
Anal Methods. 2021 Feb 7;13(5):712-718. doi: 10.1039/d0ay01712d. Epub 2021 Jan 22.
The breast cancer 1 (BRCA1) gene is a tumor suppressor gene, whose mutation is closely related to breast cancer. Therefore, the sensitive detection of the BRCA1 gene is extremely important for human health, particularly for women. In this study, a label-free fluorescent method based on hairpin DNA-templated copper nanoclusters (CuNCs) was for the first time developed for the detection of the BRCA1 gene. In the absence of target DNA, the detection system showed a strong red emission and produced a high emission peak. However, in the presence of the BRCA1 gene, the DNA probe hybridized with the BRCA1 gene and conformation of the DNA probe changed. As a result, the amount of produced CuNCs decreased and a low emission peak was obtained. The fluorescence intensity of the detection system was linearly correlated with the concentration of the BRCA1 gene ranging from 2 nM to 600 nM. The detectable limit was 2 nM for the BRCA1 gene assay, which was comparable with those reported by other non-amplifying sensors. Moreover, the developed method showed satisfactory recoveries for the BRCA1 gene assay in the bovine serum. The DNA-templated CuNC-based fluorescent assay thus offered a promising platform for the diagnosis of a breast cancer biomarker.
乳腺癌1(BRCA1)基因是一种肿瘤抑制基因,其突变与乳腺癌密切相关。因此,BRCA1基因的灵敏检测对人类健康,尤其是对女性而言极为重要。在本研究中,首次开发了一种基于发夹DNA模板化铜纳米簇(CuNCs)的无标记荧光方法用于检测BRCA1基因。在没有靶DNA的情况下,检测系统显示出强烈的红色发射并产生一个高发射峰。然而,在存在BRCA1基因的情况下,DNA探针与BRCA1基因杂交,DNA探针的构象发生变化。结果,产生的CuNCs数量减少,获得一个低发射峰。检测系统的荧光强度与BRCA1基因浓度在2 nM至600 nM范围内呈线性相关。BRCA1基因检测的可检测限为2 nM,与其他非扩增传感器报道的相当。此外,所开发的方法在牛血清中对BRCA1基因检测显示出令人满意的回收率。因此,基于DNA模板化CuNCs的荧光检测为乳腺癌生物标志物的诊断提供了一个有前景的平台。