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门控瞬态耗散二聚体 DNA 四面体纳米结构用于程序化 DNA 酶催化。

Gated Transient Dissipative Dimerization of DNA Tetrahedra Nanostructures for Programmed DNAzymes Catalysis.

机构信息

The Institute of Chemistry, The Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

出版信息

ACS Nano. 2022 Mar 22;16(3):3625-3636. doi: 10.1021/acsnano.1c06117. Epub 2022 Feb 20.

Abstract

Transient dissipative dimerization and transient gated dimerization of DNA tetrahedra nanostructures are introduced as functional modules to emulate transient and gated protein-protein interactions and emergent protein-protein guided transient catalytic functions, operating in nature. Four tetrahedra are engineered to yield functional modules that, in the presence of pre-engineered auxiliary nucleic acids and the nicking enzyme Nt.BbvCI, lead to the fueled transient dimerization of two pairs of tetrahedra. The dynamic transient formation and depletion of DNA tetrahedra are followed by transient FRET signals generated by fluorophore-labeled tetrahedra. The integration of two inhibitors within the mixture of the four tetrahedra and two auxiliary modules, fueling the transient dimerization, results in selective inhibitor-guided gated transient dimerization of two different DNA tetrahedra dimers. Kinetic models for the dynamic transient dimerization and gated transient dimerization of the DNA tetrahedra are formulated and computationally simulated. The derived rate-constants allow the prediction and subsequent experimental validation of the performance of the systems under different auxiliary conditions. In addition, by appropriate modification of the four tetrahedra structures, the triggered gated emergence of selective transient catalytic functions driven by the two pairs of DNA tetrahedra dimers is demonstrated.

摘要

DNA 四面体纳米结构的瞬态耗散二聚化和瞬态门控二聚化为模拟瞬态和门控蛋白-蛋白相互作用以及新兴的蛋白-蛋白引导的瞬态催化功能提供了功能模块,这些功能在自然界中运行。设计了四个四面体以产生功能模块,在预设计的辅助核酸和切口酶 Nt.BbvCI 的存在下,导致两对四面体的燃料驱动瞬态二聚化。通过荧光标记四面体产生的瞬态 FRET 信号来跟踪 DNA 四面体的动态瞬态形成和耗尽。在混合物中整合两个抑制剂四个四面体和两个辅助模块中,燃料瞬态二聚化,导致两种不同的 DNA 四面体二聚体的选择性抑制剂引导的门控瞬态二聚化。为 DNA 四面体的动态瞬态二聚化和门控瞬态二聚化制定了动力学模型,并进行了计算模拟。推导的速率常数允许在不同辅助条件下预测和随后验证系统的性能。此外,通过适当修改四面体结构,证明了由两对 DNA 四面体二聚体驱动的选择性瞬态催化功能的触发门控出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/8945371/f3f9d23247fe/nn1c06117_0001.jpg

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