Division of Physical Biology & Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences , Shanghai 201800, China.
ACS Appl Mater Interfaces. 2014 Oct 22;6(20):17944-53. doi: 10.1021/am5047735. Epub 2014 Oct 9.
Microarrays of biomolecules have greatly promoted the development of the fields of genomics, proteomics, and clinical assays because of their remarkably parallel and high-throughput assay capability. Immobilization strategies for biomolecules on a solid support surface play a crucial role in the fabrication of high-performance biological microarrays. In this study, rationally designed DNA tetrahedra carrying three amino groups and one single-stranded DNA extension were synthesized by the self-assembly of four oligonucleotides, followed by high-performance liquid chromatography purification. We fabricated DNA tetrahedron-based microarrays by covalently coupling the DNA tetrahedron onto glass substrates. After their biorecognition capability was evaluated, DNA tetrahedron microarrays were utilized for the analysis of different types of bioactive molecules. The gap hybridization strategy, the sandwich configuration, and the engineering aptamer strategy were employed for the assay of miRNA biomarkers, protein cancer biomarkers, and small molecules, respectively. The arrays showed good capability to anchor capture biomolecules for improving biorecognition. Addressable and high-throughput analysis with improved sensitivity and specificity had been achieved. The limit of detection for let-7a miRNA, prostate specific antigen, and cocaine were 10 fM, 40 pg/mL, and 100 nM, respectively. More importantly, we demonstrated that the microarray platform worked well with clinical serum samples and showed good relativity with conventional chemical luminescent immunoassay. We have developed a novel approach for the fabrication of DNA tetrahedron-based microarrays and a universal DNA tetrahedron-based microarray platform for the detection of different types of bioactive molecules. The microarray platform shows great potential for clinical diagnosis.
生物分子微阵列由于其显著的平行和高通量检测能力,极大地推动了基因组学、蛋白质组学和临床检测领域的发展。生物分子在固体支撑表面上的固定化策略在高性能生物微阵列的制备中起着至关重要的作用。在本研究中,通过四个寡核苷酸的自组装合成了携带三个氨基和一个单链 DNA 延伸的理性设计的 DNA 四面体,然后通过高效液相色谱纯化。我们通过将 DNA 四面体共价偶联到玻璃基底上来制造 DNA 四面体基微阵列。在评估了它们的生物识别能力之后,我们利用 DNA 四面体微阵列分析了不同类型的生物活性分子。采用缺口杂交策略、三明治构型和工程适体策略分别用于 miRNA 生物标志物、蛋白质癌症生物标志物和小分子的检测。该阵列具有良好的固定捕获生物分子的能力,可提高生物识别能力。实现了可寻址和高通量分析,具有更高的灵敏度和特异性。miRNA 标志物 let-7a、前列腺特异性抗原和可卡因的检测限分别为 10 fM、40 pg/mL 和 100 nM。更重要的是,我们证明了该微阵列平台在临床血清样本中表现良好,并且与传统的化学发光免疫分析具有良好的相关性。我们已经开发了一种基于 DNA 四面体的微阵列的新型制造方法和一种通用的基于 DNA 四面体的微阵列平台,用于检测不同类型的生物活性分子。该微阵列平台在临床诊断中具有很大的应用潜力。