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用于途径增强的合成支架。

Synthetic scaffolds for pathway enhancement.

机构信息

Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19716, United States.

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei City, Taiwan.

出版信息

Curr Opin Biotechnol. 2015 Dec;36:98-106. doi: 10.1016/j.copbio.2015.08.009. Epub 2015 Aug 29.

Abstract

Controlling local concentrations of reactants, intermediates, and enzymes in synthetic pathways is critical for achieving satisfactory productivity of any desired products. An emerging approach to exert control over local concentrations is the use of synthetic biomolecular scaffolds to co-localize key molecules of synthetic pathways. These scaffolds bring the key molecules into close proximity by recruiting pathway enzymes via ligand binding and/or physically sequestrating enzymes and metabolites into isolated compartments. Novel scaffolds made of proteins, nucleic acids, and micro-compartments with increasingly complex architecture have recently been explored and applied to a variety of pathways, with varying degrees of success. Despite these strides, precise assembly of synthetic scaffolds remains a difficult task, particularly in vivo, where interactions both intended and unexpected can lead to unpredictable results. Additionally, because heterologous enzymes often have lowered activities in their new hosts, an ideal scaffold should provide a flexible platform that can adapt to kinetic imbalances in different contexts. In this review, we discuss some of the notable advances in the creation of these synthetic scaffolds and highlight the current challenges in their application.

摘要

控制合成途径中反应物、中间产物和酶的局部浓度对于实现任何所需产物的令人满意的生产力至关重要。一种新兴的控制局部浓度的方法是使用合成生物分子支架来共定位合成途径的关键分子。这些支架通过配体结合招募途径酶,或者通过物理隔离酶和代谢物到隔离隔室,将关键分子紧密地聚集在一起。最近已经探索并应用了由蛋白质、核酸和微隔室组成的具有越来越复杂结构的新型支架,取得了不同程度的成功。尽管取得了这些进展,但精确组装合成支架仍然是一项艰巨的任务,特别是在体内,其中预期和意外的相互作用可能导致不可预测的结果。此外,由于异源酶在新宿主中的活性通常较低,理想的支架应该提供一个灵活的平台,可以适应不同环境中的动力学失衡。在这篇综述中,我们讨论了这些合成支架的一些显著进展,并强调了它们应用中的当前挑战。

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