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一个由正交核糖体与信使核糖核酸对组成的网络。

A network of orthogonal ribosome x mRNA pairs.

作者信息

Rackham Oliver, Chin Jason W

机构信息

Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.

出版信息

Nat Chem Biol. 2005 Aug;1(3):159-66. doi: 10.1038/nchembio719. Epub 2005 Jul 17.

Abstract

Synthetic biology promises the ability to program cells with new functions. Simple oscillators, switches, logic functions, cell-cell communication and pattern-forming circuits have been created by the connection of a small set of natural transcription factors and their binding sites in different ways to produce different networks of molecular interactions. However, the controlled synthesis of more complex synthetic networks and functions will require an expanded set of functional molecules with known molecular specificities. Here, we tailored the molecular specificity of duplicated Escherichia coli ribosome x mRNA pairs with respect to the wild-type ribosome and mRNAs to produce multiple orthogonal ribosome x orthogonal mRNA pairs that can process information in parallel with, but independent of, their wild-type progenitors. In these pairs, the ribosome exclusively translates the orthogonal mRNA, and the orthogonal mRNA is not a substrate for cellular ribosomes. We predicted and measured the network of interactions between orthogonal ribosomes and orthogonal mRNAs, and showed that they can be used to post-transcriptionally program the cell with Boolean logic.

摘要

合成生物学有望实现对细胞进行新功能编程的能力。通过以不同方式连接一小部分天然转录因子及其结合位点来创建简单的振荡器、开关、逻辑功能、细胞间通信和模式形成电路,从而产生不同的分子相互作用网络。然而,要实现更复杂的合成网络和功能的可控合成,将需要一套更广泛的具有已知分子特异性的功能分子。在这里,我们针对野生型核糖体和信使核糖核酸(mRNA)对重复的大肠杆菌核糖体x mRNA对的分子特异性进行了调整,以产生多个正交核糖体x正交mRNA对,这些对能够与它们的野生型祖先并行但独立地处理信息。在这些对中,核糖体专门翻译正交mRNA,而正交mRNA不是细胞核糖体的底物。我们预测并测量了正交核糖体和正交mRNA之间的相互作用网络,并表明它们可用于通过布尔逻辑对细胞进行转录后编程。

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