Department of Applied Physics, Division of Biological Physics, Chalmers University of Technology, Göteborg, Sweden.
Nano Lett. 2010 Feb 10;10(2):732-7. doi: 10.1021/nl904208y.
We report on a mass-spectrometry (time-of-flight secondary ion mass spectrometry, TOF-SIMS) based method for multiplexed DNA detection utilizing a random array, where the lipid composition of small unilamellar liposomes act as chemical barcodes to identify unique DNA target sequences down to the single molecule level. In a sandwich format, suspended target-DNA to be detected mediates the binding of capture-DNA modified liposomes to surface-immobilized probe-DNA. With the lipid composition of each liposome encoding a unique target-DNA sequence, TOF-SIMS analysis was used to determine the chemical fingerprint of the bound liposomes. Using high-resolution TOF-SIMS imaging, providing sub-200 nm spatial resolution, single DNA targets could be detected and identified via the chemical fingerprint of individual liposomes. The results also demonstrate the capability of TOF-SIMS to provide multiplexed detection of DNA targets on substrate areas in the micrometer range. Together with a high multiplexing capacity, this makes the concept an interesting alternative to existing barcode concepts based on fluorescence, Raman, or graphical codes for small-scale bioanalysis.
我们报告了一种基于质谱(飞行时间二次离子质谱,TOF-SIMS)的多重 DNA 检测方法,该方法利用随机阵列,其中小单层脂质体的脂质组成充当化学条码,可在单分子水平上识别独特的 DNA 靶序列。在夹心模式下,悬浮的靶 DNA 介导修饰的捕获 DNA 脂质体与表面固定的探针 DNA 结合。由于每个脂质体的脂质组成都编码独特的靶 DNA 序列,因此可以使用 TOF-SIMS 分析来确定结合脂质体的化学指纹。通过高分辨率 TOF-SIMS 成像,提供亚 200nm 的空间分辨率,可以通过单个脂质体的化学指纹来检测和识别单个 DNA 靶标。结果还证明了 TOF-SIMS 有能力在亚微米范围内的基质区域上进行多重 DNA 靶标的检测。结合高多重检测能力,这使得该概念成为现有基于荧光、拉曼或图形码的小型生物分析的条码概念的一个有趣替代方案。