State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, The Key Lab of Health Chemistry and Molecular Diagnosis of Suzhou, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, P.R. China.
Angew Chem Int Ed Engl. 2016 Feb 24;55(9):3073-6. doi: 10.1002/anie.201509726. Epub 2015 Dec 22.
Molecular imaging is an essential tool for disease diagnostics and treatment. Direct imaging of low-abundance nucleic acids in living cells remains challenging because of the relatively low sensitivity and insufficient signal-to-background ratio of conventional molecular imaging probes. Herein, we report a class of DNA-templated gold nanoparticle (GNP)-quantum dot (QD) assembly-based probes for catalytic imaging of cancer-related microRNAs (miRNA) in living cells with signal amplification capacity. We show that a single miRNA molecule could catalyze the disassembly of multiple QDs with the GNP through a DNA-programmed thermodynamically driven entropy gain process, yielding significantly amplified QD photoluminescence (PL) for miRNA imaging. By combining the robust PL of QDs with the catalytic amplification strategy, three orders of magnitude improvement in detection sensitivity is achieved in comparison with non-catalytic imaging probe, which enables facile and accurate differentiation between cancer cells and normal cells by miRNA imaging in living cells.
分子成像技术是疾病诊断和治疗的重要工具。由于传统分子成像探针的灵敏度相对较低,信号与背景比不足,因此直接在活细胞中对低丰度核酸进行成像仍然具有挑战性。在此,我们报告了一类基于 DNA 模板的金纳米粒子(GNP)-量子点(QD)组装的探针,用于在活细胞中具有信号放大能力的催化成像癌症相关 microRNA(miRNA)。我们表明,单个 miRNA 分子可以通过 DNA 编程的热力学驱动熵增过程催化多个 QD 与 GNP 的解组装,从而产生显著放大的 QD 光致发光(PL),用于 miRNA 成像。通过将 QD 的强 PL 与催化扩增策略相结合,与非催化成像探针相比,检测灵敏度提高了三个数量级,从而可以通过活细胞中的 miRNA 成像轻松准确地区分癌细胞和正常细胞。
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