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合成细胞中RNA折纸细胞骨架的遗传编码与表达。

Genetic encoding and expression of RNA origami cytoskeletons in synthetic cells.

作者信息

Tran Mai P, Chakraborty Taniya, Poppleton Erik, Monari Luca, Illig Maja, Giessler Franziska, Göpfrich Kerstin

机构信息

Biophysical Engineering Group, Heidelberg University, Center for Molecular Biology of Heidelberg University (ZMBH), Heidelberg, Germany.

Biophysical Engineering Group, Max Planck Institute for Medical Research, Heidelberg, Germany.

出版信息

Nat Nanotechnol. 2025 May;20(5):664-671. doi: 10.1038/s41565-025-01879-3. Epub 2025 Mar 17.

DOI:10.1038/s41565-025-01879-3
PMID:40097648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12095062/
Abstract

Bottom-up synthetic biology seeks to engineer a cell from molecular building blocks. Using DNA nanotechnology, building blocks, such as cytoskeletons, have been reverse-engineered. However, DNA nanostructures rely on chemical synthesis and thermal annealing, and therefore synthetic cells cannot produce them from their constituents such as nucleotides. Here we introduce RNA origami cytoskeleton mimics as alternative nucleic acid-based molecular hardware for synthetic cells, which we express directly inside giant unilamellar lipid vesicles (GUVs) containing a DNA template and a polymerase, chemically fuelled by feeding nucleotides from the outside. We designed RNA origami tiles that fold upon transcription and self-assemble into micrometre-long, three-dimensional RNA origami nanotubes under isothermal conditions. We observe that sequence mutations on the DNA template lead to RNA origami nanotubes and closed-ring phenotypes. Molecular dynamics simulations show that these phenotypic transitions are governed by alterations in the stability of RNA secondary structures. In addition, we achieve cortex formation with aptamer-functionalized RNA nanotubes and show that nanotube polymerization leads to membrane deformation. Altogether, our data suggest that the expression of RNA origami-based hardware will help to explore active, evolvable and RNA-based synthetic cells.

摘要

自下而上的合成生物学旨在从分子构建模块构建细胞。利用DNA纳米技术,诸如细胞骨架等构建模块已被逆向工程化。然而,DNA纳米结构依赖化学合成和热退火,因此合成细胞无法从其核苷酸等成分中产生它们。在此,我们引入RNA折纸细胞骨架模拟物,作为合成细胞基于核酸的替代分子硬件,我们将其直接表达在含有DNA模板和聚合酶的巨型单层脂质囊泡(GUVs)内部,通过从外部提供核苷酸进行化学供能。我们设计了在转录时折叠并在等温条件下自组装成微米长的三维RNA折纸纳米管的RNA折纸片。我们观察到DNA模板上的序列突变会导致RNA折纸纳米管和闭环表型。分子动力学模拟表明,这些表型转变受RNA二级结构稳定性变化的支配。此外,我们利用适配体功能化的RNA纳米管实现了皮层形成,并表明纳米管聚合会导致膜变形。总之,我们的数据表明基于RNA折纸的硬件表达将有助于探索活性、可进化且基于RNA的合成细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/1e971158c433/41565_2025_1879_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/f5457cc17419/41565_2025_1879_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/778cb0d65970/41565_2025_1879_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/7a55fda46a0b/41565_2025_1879_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/d6ab994dabde/41565_2025_1879_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/1e971158c433/41565_2025_1879_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/f5457cc17419/41565_2025_1879_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/778cb0d65970/41565_2025_1879_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/7a55fda46a0b/41565_2025_1879_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/d6ab994dabde/41565_2025_1879_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5df/12095062/1e971158c433/41565_2025_1879_Fig5_HTML.jpg

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