DNA Electronics Ltd., London, UK.
Nat Methods. 2013 Jul;10(7):641-6. doi: 10.1038/nmeth.2520. Epub 2013 Jun 9.
We developed an integrated chip for real-time amplification and detection of nucleic acid using pH-sensing complementary metal-oxide semiconductor (CMOS) technology. Here we show an amplification-coupled detection method for directly measuring released hydrogen ions during nucleotide incorporation rather than relying on indirect measurements such as fluorescent dyes. This is a label-free, non-optical, real-time method for detecting and quantifying target sequences by monitoring pH signatures of native amplification chemistries. The chip has ion-sensitive field effect transistor (ISFET) sensors, temperature sensors, resistive heating, signal processing and control circuitry all integrated to create a full system-on-chip platform. We evaluated the platform using two amplification strategies: PCR and isothermal amplification. Using this platform, we genotyped and discriminated unique single-nucleotide polymorphism (SNP) variants of the cytochrome P450 family from crude human saliva. We anticipate this semiconductor technology will enable the creation of devices for cost-effective, portable and scalable real-time nucleic acid analysis.
我们开发了一种使用 pH 感应互补金属氧化物半导体 (CMOS) 技术实时扩增和检测核酸的集成芯片。在这里,我们展示了一种扩增偶联检测方法,用于直接测量核苷酸掺入过程中释放的氢离子,而不是依赖于荧光染料等间接测量方法。这是一种无标记、非光学、实时的方法,通过监测天然扩增化学物质的 pH 特征来检测和定量目标序列。该芯片具有离子敏感场效应晶体管 (ISFET) 传感器、温度传感器、电阻加热、信号处理和控制电路,所有这些都集成在一个完整的片上系统平台中。我们使用两种扩增策略——PCR 和等温扩增来评估该平台。使用该平台,我们从粗人唾液中对细胞色素 P450 家族的独特单核苷酸多态性 (SNP) 变体进行了基因分型和区分。我们预计这种半导体技术将能够创建用于经济高效、便携式和可扩展的实时核酸分析的设备。