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利用 DNA 编程蛋白质聚合。

Programming Protein Polymerization with DNA.

出版信息

J Am Chem Soc. 2018 Nov 21;140(46):15950-15956. doi: 10.1021/jacs.8b10011. Epub 2018 Nov 8.

DOI:10.1021/jacs.8b10011
PMID:30407003
Abstract

A strategy that utilizes DNA for controlling the association pathway of proteins is described. This strategy uses sequence-specific DNA interactions to program energy barriers for polymerization, allowing for either step-growth or chain-growth pathways to be accessed. Two sets of mutant green fluorescent protein (mGFP)-DNA monomers with single DNA modifications have been synthesized and characterized. Depending on the deliberately controlled sequence and conformation of the appended DNA, these monomers can be polymerized through either a step-growth or chain-growth pathway. Cryo-electron microscopy with Volta phase plate technology enables the visualization of the distribution of the oligomer and polymer products, and even the small mGFP-DNA monomers. Whereas cyclic and linear polymer distributions were observed for the step-growth DNA design, in the case of the chain-growth system linear chains exclusively were observed, and a dependence of the chain length on the concentration of the initiator strand was noted. Importantly, the chain-growth system possesses a living character whereby chains can be extended with the addition of fresh monomer. This work represents an important and early example of mechanistic control over protein assembly, thereby establishing a robust methodology for synthesizing oligomeric and polymeric protein-based materials with exceptional control over architecture.

摘要

描述了一种利用 DNA 控制蛋白质缔合途径的策略。该策略使用序列特异性 DNA 相互作用来为聚合编程能量势垒,从而可以访问逐步或链式生长途径。已经合成并表征了两组具有单个 DNA 修饰的突变型绿色荧光蛋白 (mGFP)-DNA 单体。根据附加 DNA 的精心控制的序列和构象,这些单体可以通过逐步或链式生长途径聚合。使用带有 Volta 相板技术的冷冻电子显微镜可以可视化寡聚物和聚合物产物的分布,甚至可以观察到小的 mGFP-DNA 单体。对于逐步生长 DNA 设计,观察到了环状和线性聚合物分布,而在链式生长系统中,仅观察到线性链,并且注意到链长与引发剂链浓度的依赖性。重要的是,链式生长系统具有活性特征,通过添加新鲜单体可以延长链。这项工作代表了对蛋白质组装的机制控制的一个重要的早期例子,从而为合成具有出色结构控制的寡聚和聚合蛋白基材料建立了一种强大的方法。

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