Cell-Free PURE System: Evolution and Achievements

Author:

Cui Yi12,Chen Xinjie1,Wang Ze2,Lu Yuan1ORCID

Affiliation:

1. Key Laboratory of Industrial Biocatalysis, Ministry of Education, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China

2. College of Life Sciences, Shenyang Normal University, Shenyang 110034, Liaoning, China

Abstract

The cell-free protein synthesis (CFPS) system, as a technical core of synthetic biology, can simulate the transcription and translation process in an in vitro open environment without a complete living cell. It has been widely used in basic and applied research fields because of its advanced engineering features in flexibility and controllability. Compared to a typical crude extract-based CFPS system, due to defined and customizable components and lacking protein-degrading enzymes, the protein synthesis using recombinant elements (PURE) system draws great attention. This review first discusses the elemental composition of the PURE system. Then, the design and preparation of functional proteins for the PURE system, especially the critical ribosome, were examined. Furthermore, we trace the evolving development of the PURE system in versatile areas, including prototyping, synthesis of unnatural proteins, peptides and complex proteins, and biosensors. Finally, as a state-of-the-art engineering strategy, this review analyzes the opportunities and challenges faced by the PURE system in future scientific research and diverse applications.

Funder

Tsinghua University

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Self-lysis microbial consortia for predictable multi-proteins assembly;Bioorganic Chemistry;2024-03

2. From Cells to Cell-Free Platforms;Advances in Bioinformatics and Biomedical Engineering;2023-10-02

3. The Hidden Biocatalytic Potential of the Old Yellow Enzyme Family;2023-07-11

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