Song Joon Myong, Yang Min-Sung, Kwan Ho Taik
Research Institute of Pharmaceutical Sciences and College of Pharmacy, Seoul National University, Seoul 151-742, South Korea.
Biosens Bioelectron. 2007 Feb 15;22(7):1447-53. doi: 10.1016/j.bios.2006.06.026. Epub 2006 Aug 4.
We have applied an integrated circuit photodiode array (PDA) chip system to a DNA chip. The PDA chip system, constructed using conventional bipolar semiconductor technology, acts as a solid transducer surface as well as a two-dimensional photodetector. DNA hybridization was performed directly on the PDA chip. The target DNA, the Bacillus subtilis sspE gene, was amplified by polymerase chain reaction (PCR). The 340-bp PCR product was labeled using digoxigenin (DIG). A silicon nitride layer on the photodiode was treated with poly-L-lysine to immobilize the DNA on the surface of the photodiode detection elements. Consequently, the surface of the photodiode detector became positively charged. An anti-DIG-alkaline phosphatase conjugate was reacted with the hybridized DIG-labeled DNA. A color reaction was performed based on the enzymatic reaction between nitroblue tetrazolium/5-bromo-4-chloro-3-indolyl-phosphate (NBT/BCIP) staining solution and a DNA complex containing antibodies. A blue precipitate was formed on the surfaces of the photodiode detection elements. Successful quantitative analysis of the hybridized PCR products was achieved from the light absorption properties of the blue enzymatic reaction product that was produced after a series of reaction processes. Our DNA chip system avoids the complicated optical alignments and light-collecting optical components that are usually required for an optical DNA chip device. As a result, a simple, compact, portable and low-cost DNA chip is achieved. This system has great potential as an alternative system to the conventional DNA reader.
我们已将一种集成电路光电二极管阵列(PDA)芯片系统应用于DNA芯片。该PDA芯片系统采用传统的双极半导体技术构建,既作为固体换能器表面,又作为二维光电探测器。DNA杂交直接在PDA芯片上进行。目标DNA,即枯草芽孢杆菌sspE基因,通过聚合酶链反应(PCR)进行扩增。340碱基对的PCR产物用洋地黄毒苷(DIG)进行标记。光电二极管上的氮化硅层用聚-L-赖氨酸处理,以便将DNA固定在光电二极管检测元件的表面。结果,光电二极管探测器的表面带正电。抗DIG碱性磷酸酶共轭物与杂交的DIG标记DNA发生反应。基于硝基蓝四唑/5-溴-4-氯-3-吲哚磷酸(NBT/BCIP)染色溶液与含抗体的DNA复合物之间的酶促反应进行显色反应。在光电二极管检测元件的表面形成蓝色沉淀。通过一系列反应过程后产生的蓝色酶促反应产物的光吸收特性,成功实现了对杂交PCR产物的定量分析。我们的DNA芯片系统避免了光学DNA芯片装置通常所需的复杂光学对准和光收集光学元件。结果,实现了一种简单、紧凑、便携且低成本的DNA芯片。该系统作为传统DNA读取器的替代系统具有巨大潜力。