Laboratory for Characterization and Processing of Polymers, University of Maribor, Smetanova ulica 17, 2000 Maribor, Slovenia.
Institute of Chemistry, University of Graz, Heinrichstraße 28/3, 8010 Graz, Austria.
Biosens Bioelectron. 2015 Jun 15;68:437-441. doi: 10.1016/j.bios.2015.01.038. Epub 2015 Jan 17.
DNA immobilization for the manufacturing of microarrays requires sufficient probe density, low unspecific binding and high interaction efficiency with complementary strands that are detected from solutions. Many of these important parameters are affected by the surface chemistry and the blocking steps conducted during DNA spotting and hybridization. This work describes an alternative method to selectively immobilize probes and to detect DNA on biocompatible, hydrophilic cellulose coated supports with low unspecific binding, high selectivity and appropriate sensitivity. It takes advantage of a relatively selective adsorption of water soluble polysaccharides on a solid cellulose matrix. Single strands of DNA were conjugated to this soluble polysaccharide and subsequently micro-spotted on solid cellulose thin films that were coated on glass and polymer slides. This resulted in adsorptively bound DNA-probes that were used to detect complementary, labelled DNA strands with different lengths and sequences by hybridization. The interaction of the DNA-conjugates with cellulose surfaces and the selectivity of hybridization were investigated by a quartz crystal microbalance with dissipation monitoring (QCM-D) and fluorescence scanning. The method of non-covalent immobilization of DNA probes on an uncharged, non-reactive, hydrophilic support lowers the unspecific binding and the number of handling steps required to conduct the experiments for the detection of DNA on microarrays. Simultaneously selectivity, hybridization efficiency and detection limits are maintained.
DNA 固定化用于制造微阵列需要足够的探针密度、低非特异性结合和与从溶液中检测到的互补链的高相互作用效率。这些重要参数中的许多都受到 DNA 点样和杂交过程中表面化学和封闭步骤的影响。本工作描述了一种替代方法,可选择性地固定探针,并在具有低非特异性结合、高选择性和适当灵敏度的生物相容性、亲水性纤维素涂层载体上检测 DNA。它利用了水溶性多糖在固体纤维素基质上的相对选择性吸附。单链 DNA 与这种可溶性多糖结合,然后微点样到涂覆在玻璃和聚合物载玻片上的固体纤维素薄膜上。这导致了吸附结合的 DNA 探针,可用于通过杂交检测具有不同长度和序列的互补标记 DNA 链。通过石英晶体微天平(QCM-D)和荧光扫描研究了 DNA 缀合物与纤维素表面的相互作用和杂交的选择性。非共价固定化 DNA 探针在不带电荷、无反应性、亲水性载体上的方法降低了非特异性结合和进行微阵列上 DNA 检测所需的操作步骤数量。同时保持了选择性、杂交效率和检测限。