Center for Research at the Bio/Nano Interface, Department of Chemistry, UF Genetics Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
Anal Chem. 2009 Aug 15;81(16):7009-14. doi: 10.1021/ac9011073.
To facilitate the selection of effective therapeutic pathways and improve clinical outcomes, sensitive and simultaneous diagnosis of multiple trace biomarkers or cancer cells from complex living samples is particularly critical in the early stages of tumor development. To achieve this, we have combined the selectivity and affinity of aptamers with the spectroscopic advantages of fluorescence resonance energy transfer (FRET) nanoparticles (NPs). This has produced an aptamer-conjugated FRET NP assay that performs simultaneous multiplexed monitoring of cancer cells with the desired degree of sensitivity and selectivity. First, by changing the doping ratio of three different dyes, the FRET-mediated emission signatures could be tuned such that the nanoparticles would exhibit multiple colors upon excitation with a single wavelength. These FRET nanoparticles were then modified by a few aptamers specific for different cancer cell lines, in this case, T-cell leukemia and B-cell lymphoma. As a result, simultaneous and sensitive detection of multiple cancer cell targets was achieved. Therefore, our aptamer-conjugated FRET NPs are highly promising for potential applications in the sensitive monitoring of multiple cancer cells for biomedical research and medical diagnostics.
为了促进有效治疗途径的选择和改善临床结果,在肿瘤发展的早期阶段,从复杂的活体样本中灵敏且同时诊断多种痕量生物标志物或癌细胞尤为关键。为此,我们将适体的选择性和亲和力与荧光共振能量转移(FRET)纳米粒子(NPs)的光谱优势相结合。这产生了一种适体偶联的 FRET NP 测定法,可同时以所需的灵敏度和选择性对癌细胞进行多重监测。首先,通过改变三种不同染料的掺杂比,可以调整 FRET 介导的发射特征,使得纳米粒子在单个波长的激发下会呈现出多种颜色。然后,通过少数几种针对不同癌细胞系的适体对这些 FRET 纳米粒子进行修饰,在这种情况下,是 T 细胞白血病和 B 细胞淋巴瘤。结果,实现了对多种癌细胞靶标的同时灵敏检测。因此,我们的适体偶联的 FRET NPs 非常有希望在用于生物医学研究和医学诊断的多种癌细胞的灵敏监测中得到应用。