Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran; Department of Pharmaceutical Biomaterials and Medical Biomaterials Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
J Pharm Biomed Anal. 2018 Apr 15;152:81-88. doi: 10.1016/j.jpba.2018.01.014. Epub 2018 Jan 9.
BRCA1 (breast cancer 1) genomic deletions are the most important founder mutations in breast cancer patients and can be passed to you from your mother or father. Herein, we report a silver nanoclusters-based (AgNCs-based) fluorescence resonance energy transfer (FRET) method for detection of BRCA1 gene deletion. The method relies on the specific hybridization of DNA-AgNCs fluorescent probe to deleted genes and interaction between double stranded DNA-AgNCs and QD, and the signal amplification through energy transfer from fluorescent AgNCs to QDs during FRET. Such fabricated QDs/DNA-AgNCs interaction might be beneficial for the nanomaterials based biosensing methods Under best possible conditions a linear correlation was established between the fluorescence intensity and the concentration of deletion sequence in the range of 5.0 × 10-1.0 × 10 M with a detection limit of 1.2 × 10 M. Using this method, we could effectively determine gene deletions by using the nonamplified genomic DNAs that were extracted from the MCF-7 as a breast cancer cell line.
BRCA1(乳腺癌 1 号)基因组缺失是乳腺癌患者最重要的种系突变,可能是从你的母亲或父亲那里遗传给你的。在此,我们报告了一种基于银纳米团簇(AgNCs)的荧光共振能量转移(FRET)方法,用于检测 BRCA1 基因缺失。该方法依赖于 DNA-AgNCs 荧光探针与缺失基因的特异性杂交,以及双链 DNA-AgNCs 与 QD 之间的相互作用,并通过 FRET 过程中荧光 AgNCs 向 QD 的能量转移进行信号放大。这种制造的 QD/DNA-AgNCs 相互作用可能有利于基于纳米材料的生物传感方法。在最佳条件下,荧光强度与缺失序列浓度在 5.0×10-1.0×10 M 范围内呈线性相关,检测限为 1.2×10 M。使用该方法,我们可以使用从 MCF-7 作为乳腺癌细胞系提取的非扩增基因组 DNA 有效地确定基因缺失。