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Proton gradients from light-harvesting E. coli control DNA assemblies for synthetic cells.来自聚光大肠杆菌的质子梯度控制用于合成细胞的 DNA 组装体。
Nat Commun. 2021 Jun 25;12(1):3967. doi: 10.1038/s41467-021-24103-x.
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Gene duplication and subsequent diversification strongly affect phenotypic evolvability and robustness.基因复制及随后的多样化对表型可塑性和稳健性有强烈影响。
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Division and Regrowth of Phase-Separated Giant Unilamellar Vesicles*.相分离的巨型单室泡囊的分裂和再生*。
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Roadmap to Building a Cell: An Evolutionary Approach.构建细胞的路线图:一种进化方法。
Front Bioeng Biotechnol. 2020 Aug 19;8:927. doi: 10.3389/fbioe.2020.00927. eCollection 2020.
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Barcoded DNA origami structures for multiplexed optimization and enrichment of DNA-based protein-binding cavities.条形码 DNA 折纸结构用于基于 DNA 的蛋白质结合腔的多重优化和富集。
Nat Chem. 2020 Sep;12(9):852-859. doi: 10.1038/s41557-020-0504-6. Epub 2020 Jul 13.
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Evolution of interface binding strengths in simplified model of protein quaternary structure.蛋白质四级结构简化模型中界面结合强度的演变。
PLoS Comput Biol. 2019 Jun 3;15(6):e1006886. doi: 10.1371/journal.pcbi.1006886. eCollection 2019 Jun.
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Mastering Complexity: Towards Bottom-up Construction of Multifunctional Eukaryotic Synthetic Cells.掌握复杂性:迈向多功能真核合成细胞的自下而上构建。
Trends Biotechnol. 2018 Sep;36(9):938-951. doi: 10.1016/j.tibtech.2018.03.008. Epub 2018 Apr 21.
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Science. 2018 Jan 19;359(6373):296-301. doi: 10.1126/science.aao4284.
10
Fractal assembly of micrometre-scale DNA origami arrays with arbitrary patterns.具有任意图案的微米级 DNA 折纸阵列的分形组装。
Nature. 2017 Dec 6;552(7683):67-71. doi: 10.1038/nature24655.

基于 DNA 折纸瓦片的多联体进行基因型-表型映射。

Genotype-phenotype mapping with polyominos made from DNA origami tiles.

机构信息

Max Planck Institute for Medical Research, Biophysical Engineering Group, Heidelberg, Germany; Department of Physics and Astronomy, Heidelberg University, Heidelberg, Germany.

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

出版信息

Biophys J. 2022 Dec 20;121(24):4840-4848. doi: 10.1016/j.bpj.2022.09.006. Epub 2022 Sep 10.

DOI:10.1016/j.bpj.2022.09.006
PMID:36088535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9811662/
Abstract

The correlation between genetic information and characteristics of a living cell-its genotype and its phenotype-constitutes the basis of genetics. Here, we experimentally realize a primitive form of genotype-phenotype mapping with DNA origami. The DNA origami can polymerize into two-dimensional lattices (phenotype) via blunt-end stacking facilitated by edge staples at the seam of the planar DNA origami. There are 80 binding positions for edge staples, which allow us to translate an 80-bit long binary code (genotype) onto the DNA origami. The presence of an edge staple thus corresponds to a "1" and its absence to a "0." The interactions of our DNA-based system can be reproduced by a polyomino model. Polyomino growth simulations qualitatively reproduce our experimental results. We show that not only the absolute number of base stacks but also their sequence position determine the cluster size and correlation length of the orientation of single DNA origami within the cluster. Importantly, the mutation of a few bits can result in major morphology changes of the DNA origami cluster, while more often, major sequence changes have no impact. Our experimental realization of a correlation between binary information ("genotype") and cluster morphology ("phenotype") thus reproduces key properties of genotype-phenotype maps known from living systems.

摘要

遗传信息与活细胞特征之间的相关性——其基因型和表型——构成了遗传学的基础。在这里,我们通过 DNA 折纸术实验实现了一种原始的基因型-表型映射形式。DNA 折纸术可以通过边缘订书钉在平面 DNA 折纸术的拼接处促进的钝端堆叠,聚合形成二维晶格(表型)。边缘订书钉有 80 个结合位置,这使我们能够将 80 位长的二进制代码(基因型)转化为 DNA 折纸术。因此,边缘订书钉的存在对应于“1”,不存在对应于“0”。我们基于 DNA 的系统的相互作用可以通过多聚体模型来重现。多聚体生长模拟定性地再现了我们的实验结果。我们表明,不仅碱基堆叠的绝对数量,而且它们的序列位置决定了单个 DNA 折纸术在簇内的取向的簇大小和相关长度。重要的是,少数位的突变会导致 DNA 折纸术簇的形态发生重大变化,而更多情况下,主要的序列变化没有影响。因此,我们在二进制信息(“基因型”)和簇形态(“表型”)之间的相关性的实验实现再现了已知的活系统中基因型-表型图谱的关键性质。