Li Yougen, Cu Yen Thi Hong, Luo Dan
Department of Biological and Environmental Engineering, Cornell University, Ithaca, New York 14853-5701, USA.
Nat Biotechnol. 2005 Jul;23(7):885-9. doi: 10.1038/nbt1106. Epub 2005 Jun 12.
Rapid, multiplexed, sensitive and specific molecular detection is of great demand in gene profiling, drug screening, clinical diagnostics and environmental analysis. One of the major challenges in multiplexed analysis is to identify each specific reaction with a distinct label or 'code'. Two encoding strategies are currently used: positional encoding, in which every potential reaction is preassigned a particular position on a solid-phase support such as a DNA microarray, and reaction encoding, where every possible reaction is uniquely tagged with a code that is most often optical or particle based. The micrometer size, polydispersity, complex fabrication process and nonbiocompatibility of current codes limit their usability. Here we demonstrate the synthesis of dendrimer-like DNA-based, fluorescence-intensity-coded nanobarcodes, which contain a built-in code and a probe for molecular recognition. Their application to multiplexed detection of the DNA of several pathogens is first shown using fluorescence microscopy and dot blotting, and further demonstrated using flow cytometry that resulted in detection that was sensitive (attomole) and rapid.
快速、多重、灵敏且特异的分子检测在基因谱分析、药物筛选、临床诊断及环境分析中具有巨大需求。多重分析的主要挑战之一是用独特的标记或“编码”识别每个特定反应。目前使用两种编码策略:位置编码,即给每个潜在反应预先指定固相支持物(如DNA微阵列)上的特定位置;反应编码,即给每个可能反应用一种编码唯一标记,这种编码通常基于光学或颗粒。当前编码的微米尺寸、多分散性、复杂的制造过程及非生物相容性限制了它们的实用性。在此,我们展示了类树枝状基于DNA的荧光强度编码纳米条形码的合成,其包含一个内置编码和一个用于分子识别的探针。首先使用荧光显微镜和斑点印迹展示了它们在几种病原体DNA多重检测中的应用,并用流式细胞术进一步证明,结果显示检测灵敏(阿托摩尔)且快速。