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DNA 支架介导的邻近组装和多酶反应的限制。

DNA-Scaffolded Proximity Assembly and Confinement of Multienzyme Reactions.

机构信息

Department of Chemistry, Rutgers University-Camden, Camden, NJ, 08102, USA.

Center for Computational and Integrative Biology, Rutgers University-Camden, Camden, NJ, 08102, USA.

出版信息

Top Curr Chem (Cham). 2020 Apr 4;378(3):38. doi: 10.1007/s41061-020-0299-3.

Abstract

Cellular functions rely on a series of organized and regulated multienzyme cascade reactions. The catalytic efficiencies of these cascades depend on the precise spatial organization of the constituent enzymes, which is optimized to facilitate substrate transport and regulate activities. Mimicry of this organization in a non-living, artificial system would be very useful in a broad range of applications-with impacts on both the scientific community and society at large. Self-assembled DNA nanostructures are promising applications to organize biomolecular components into prescribed, multidimensional patterns. In this review, we focus on recent progress in the field of DNA-scaffolded assembly and confinement of multienzyme reactions. DNA self-assembly is exploited to build spatially organized multienzyme cascades with control over their relative distance, substrate diffusion paths, compartmentalization and activity actuation. The combination of addressable DNA assembly and multienzyme cascades can deliver breakthroughs toward the engineering of novel synthetic and biomimetic reactors.

摘要

细胞功能依赖于一系列有组织和调节的多酶级联反应。这些级联的催化效率取决于组成酶的精确空间组织,这种组织优化是为了促进底物运输和调节活性。在非生命的人工系统中模拟这种组织在广泛的应用中非常有用,对科学界和整个社会都有影响。自组装 DNA 纳米结构是将生物分子组件组织成预定的多维模式的有前途的应用。在这篇综述中,我们专注于 DNA 支架组装和多酶反应限制领域的最新进展。DNA 自组装被用来构建具有相对距离、底物扩散路径、分隔和活性启动控制的空间组织的多酶级联。可寻址 DNA 组装和多酶级联的结合可以为新型合成和仿生反应器的工程设计带来突破。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cede/7127875/92fa8bfefe42/41061_2020_299_Fig1_HTML.jpg

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