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A DNA Neural Network Constructed from Molecular Variable Gain Amplifiers

机译:由分子可变增益放大器构建的DNA神经网络

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Biological nucleic acids have important roles as diagnostic markers for disease. The detection of just one molecular marker, such as a DNA sequence carrying a single nucleotide variant (SNV), can sometimes be indicative of a disease state. However, a reliable diagnosis and treatment decision often requires interpreting a combination of markers via complex algorithms. Here, we describe a diagnostic technology based on DNA strand displacement that combines single nucleotide specificity with the ability to interpret the information encoded in panels of single-stranded nucleic acids through a molecular neural network computation. Our system is constructed around a single building block-a catalytic amplifier with a competitive inhibitor or 'sink.' In previous work, we demonstrated that such a system can be used to reliably detect SNVs in single stranded nucleic acids. Here, we show that these same building blocks can be reconfigured to create an amplification system with adjustable gain α. That is, the concentration of an output signal produced is exactly α times larger than the concentration of input added initially, and the value of α can be adjusted experimentally. Finally, we demonstrate that variable gain amplification and mismatch discrimination elements can be combined into a two-input neural network classifier. Together, our results suggest a novel approach for engineering molecular classifier circuits with predictable behaviors.
机译:生物核酸作为疾病的诊断标记具有重要作用。仅检测一种分子标记,例如带有单个核苷酸变异体(SNV)的DNA序列,有时可以指示疾病状态。但是,可靠的诊断和治疗决策通常需要通过复杂的算法来解释标记的组合。在这里,我们描述了一种基于DNA链置换的诊断技术,该技术结合了单核苷酸特异性和通过分子神经网络计算来解释单链核酸面板中编码信息的能力。我们的系统是围绕一个单一的构建块构建的-具有竞争性抑制剂或“水槽”的催化放大器。在以前的工作中,我们证明了这种系统可用于可靠地检测单链核酸中的SNV。在这里,我们表明可以重新配置这些相同的构建块,以创建具有可调增益α的放大系统。也就是说,产生的输出信号的浓度恰好是最初添加的输入浓度的α倍,并且α的值可以通过实验进行调整。最后,我们证明了可变增益放大和失配鉴别元素可以组合成一个两输入神经网络分类器。在一起,我们的结果提出了一种具有可预测行为的工程分子分类器电路的新方法。

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