基于模型的设计策略来设计mirna调节的检测系统。

IF 2.3
Frontiers in systems biology Pub Date : 2025-08-14 eCollection Date: 2025-01-01 DOI:10.3389/fsysb.2025.1601854
Renske J Verkuijlen, Robert W Smith
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引用次数: 0

摘要

mirna是很有前途的诊断生物标志物。这些小RNA分子一直存在于人体内,但当一个人患上某些疾病时就会失调。尽管在无细胞测试中检测这些生物标志物的工作正在进行中,但目前的系统通常只关注检测特定miRNA的存在或缺失,而不是miRNA的浓度。因此,当疾病引起的失调发生时,这些测试可能会错过miRNA浓度的相对变化。这项工作是WUR iGEM 2024项目(miRADAR)的一部分,旨在通过在无细胞诊断测试中结合miRNA浓度依赖的阈值机制来解决这一空白。在该系统中,需要将连续的miRNA输入浓度转换为二进制输出信号,将miRNA浓度划分为健康(无输出信号)或指示疾病(强输出信号)。为了帮助测试的实验工程,这里我们使用数学模型来评估和评估不同的候选网络。我们应用先前发表的多目标优化策略来获得满足相关约束的设计,例如低基础表达,高读数水平,以及在低和高输入miRNA浓度之间的陡峭切换行为。三种不同生物机制的模型根据其产生所需二进制输出信号的能力进行了比较。一种方法使用三节点蛋白质网络(如前馈回路),而另外两种方法使用基于rna的支点系统。总的来说,支点介导的链位移系统显示出最有潜力的实验实施。这些系统被认为在无细胞环境中负担较小,可以更容易地用于新的miRNA序列,并且显示出很高的检测精度。基于我们的结果,我们讨论了包含序列特定参数如何扩展我们的数学模型的设计空间,以及如何仔细地设计优化标准来评估设计。最后,我们基于模型的研究强调,在未来,支点介导的链位移网络有可能成为生物传感工具的高效miRNA检测系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A model-based design strategy to engineer miRNA-regulated detection systems.

miRNAs are promising diagnostic biomarkers. These small RNA molecules are always present in the human body but become dysregulated when a person develops certain diseases. Although the detection of these biomarkers in cell-free tests is ongoing work, current systems often focus solely on detecting the presence or absence of a specific miRNA, rather than the miRNAs concentration. Thus, these tests may miss relative changes in miRNA concentration when disease-induced dysregulation occurs. This work, part of the WUR iGEM 2024 project (miRADAR), aimed to address this gap by incorporating an miRNA concentration-dependent threshold mechanism in a cell-free diagnostic test. In this system, continuous miRNA input concentrations need to be converted into a binary output signal, classifying the miRNA concentration as healthy (no output signal) or indicative of disease (strong output signal). To aid the experimental engineering of the test, here we use mathematical models to evaluate and assess different candidate networks. We apply a previously published multi-objective optimisation strategy to obtain designs that satisfy relevant constraints, such as low basal expression, high readout levels, and steep switching behaviour between low and high input miRNA concentrations. Models for three different biological mechanisms were compared based on their ability to generate the desired binary output signal. One approach used three-node protein networks (such as feed-forward loops), while the other two utilised RNA-based toehold systems. Overall, the toehold-mediated strand displacement systems demonstrated the most potential for experimental implementation. These systems are believed to be less burdensome in a cell-free environment, can be more readily engineered for new miRNA sequences, and showed high detection accuracy. Based on our results, we discuss how the inclusion of sequence-specific parameters could expand the design space of our mathematical models and how careful engineering of optimisation criteria is required to evaluate designs. Ultimately, our model-based study highlights that toehold-mediated strand displacement networks have the potential to be efficient miRNA detection systems for biosensing tools in the future.

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