Juliette Bucci, Layla Malouf, Diana A Tanase, Nada Farag, Jacob R Lamb, Roger Rubio-Sánchez, Serena Gentile, Erica Del Grosso, Clemens F Kaminski, Lorenzo Di Michele, Francesco Ricci
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引用次数: 0
摘要
无膜区室和细胞器在调节细胞过程中的作用已得到广泛认可,因此迫切需要充分利用它们作为合成细胞的结构和功能元素的潜力。尽管进展迅速,但合成再现天然无膜细胞器的非平衡、空间分布式反应仍然遥遥无期。在这里,我们证明了核酸裂解酶的活性可以通过封存各自的 DNA 或 RNA 底物而被定位在基于 DNA 的无膜区室中。反应扩散过程会导致复杂的非平衡模式,并取决于酶的浓度。通过抑制类似的动态模式,我们将不同的底物在空间上组织成同心亚区,然后由不同的酶进行选择性处理,展示了酶活性的空间分布。除了扩大我们在合成无膜细胞器中设计先进生物仿生功能的能力外,我们的研究成果还有助于将基于 DNA 的凝结物用作微生物反应器或检测和定量酶与核酸的平台。
Membrane-less compartments and organelles are widely acknowledged for their role in regulating cellular processes, and there is an urgent need to harness their full potential as both structural and functional elements of synthetic cells. Despite rapid progress, synthetically recapitulating the nonequilibrium, spatially distributed responses of natural membrane-less organelles remains elusive. Here, we demonstrate that the activity of nucleic-acid cleaving enzymes can be localized within DNA-based membrane-less compartments by sequestering the respective DNA or RNA substrates. Reaction-diffusion processes lead to complex nonequilibrium patterns, dependent on enzyme concentration. By arresting similar dynamic patterns, we spatially organize different substrates in concentric subcompartments, which can be then selectively addressed by different enzymes, demonstrating spatial distribution of enzymatic activity. Besides expanding our ability to engineer advanced biomimetic functions in synthetic membrane-less organelles, our results may facilitate the deployment of DNA-based condensates as microbioreactors or platforms for the detection and quantitation of enzymes and nucleic acids.
期刊介绍:
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