Cardoso Ana R, Moreira Felismina T C, Fernandes Rúben, Sales M Goreti F
BioMark-CINTESIS/ISEP, School of Engineering, Polytechnic Institute of Porto, Portugal; Molecular Mechanisms of Disease Unit, Centre of Research in Health and Environment (CISA), ESTSP-IPP, Portugal.
BioMark-CINTESIS/ISEP, School of Engineering, Polytechnic Institute of Porto, Portugal.
Biosens Bioelectron. 2016 Jun 15;80:621-630. doi: 10.1016/j.bios.2016.02.035. Epub 2016 Feb 14.
This work, describes for the first time, a simple biosensing design to yield an ultrasensitive electrochemical biosensor for a cancer biomarker detection, miRNA-155, with linear response down to the attomolar range. MiRNA-155 was selected for being overexpressed in breast cancer. The biosensor was assembled in two stages: (1) the immobilization of the anti-miRNA-155 that was thiol modified on an Au-screen printed electrode (Au-SPE), followed by (2) blocking the areas of non-specific binding with mercaptosuccinic acid. Atomic force microscopy (AFM) and electrochemical techniques including cyclic voltammetry (CV), impedance spectroscopy (EIS) and square wave voltammetry (SWV) confirmed the surface modification of these devices and their ability to hybridize successfully and stably with miRNA-155. The final biosensor provided a sensitive detection of miRNA-155 from 10 aM to 1.0 nM with a low detection limit (LOD) of 5.7 aM in real human serum samples. Good results were obtained in terms of selectivity towards breast cancer antigen CA-15.3 and bovine serum albumin (BSA). Raw fluid extracts from cell-lines of melanoma did not affect the biosensor response (no significant change of the blank), while raw extracts from breast cancer yielded a positive signal against miRNA-155. This simple and sensitive strategy is a promising alternative for simultaneous quantitative analysis of multiple miRNA in physiological fluids for biomedical research and point-of-care (POC) diagnosis.
这项工作首次描述了一种简单的生物传感设计,用于制备一种超灵敏的电化学生物传感器,用于检测癌症生物标志物miRNA - 155,其线性响应低至阿托摩尔范围。选择miRNA - 155是因为它在乳腺癌中过表达。该生物传感器分两个阶段组装:(1)将硫醇修饰的抗miRNA - 155固定在金丝网印刷电极(Au - SPE)上,然后(2)用巯基琥珀酸封闭非特异性结合区域。原子力显微镜(AFM)和包括循环伏安法(CV)、阻抗谱(EIS)和方波伏安法(SWV)在内的电化学技术证实了这些器件的表面修饰以及它们与miRNA - 155成功稳定杂交的能力。最终的生物传感器能够在实际人血清样本中灵敏地检测10 aM至1.0 nM的miRNA - 155,检测限低至5.7 aM。在对乳腺癌抗原CA - 15.3和牛血清白蛋白(BSA)的选择性方面取得了良好结果。黑色素瘤细胞系的原液提取物不影响生物传感器的响应(空白无显著变化),而乳腺癌的原液提取物对miRNA - 155产生阳性信号。这种简单而灵敏的策略是用于生物医学研究和即时检测(POC)诊断的生理流体中多种miRNA同时定量分析的一种有前景的替代方法。