活性T7 RNA聚合酶的规模化无细胞生产

IF 3.6 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Ryan N. Rezvani, Rochelle Aw, Wei Chan, Krishnathreya Satish, Han Chen, Adi Lavy, Swechha Rimal, Divyesh A. Patel, Govind Rao, James R. Swartz, Matthew P. DeLisa, Erik Kvam, Ashty S. Karim, Antje Krüger, Weston Kightlinger, Michael C. Jewett
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引用次数: 0

摘要

SARS-CoV-2大流行凸显了对强大、快速的生物制造模式的迫切需求。在这里,我们展示了T7 RNA聚合酶的快速工艺开发和可扩展的无细胞生产,T7 RNA聚合酶是mRNA疫苗合成的关键成分。我们进行了1-L无细胞基因表达(CFE)反应,纯度超过90%,内毒素水平低,相对于商业T7 RNA聚合酶的活性增强。为了实现这一演示,我们实施了滚动圈扩增来克服DNA模板生成的困难,并调整无细胞反应条件,如温度、添加剂、纯化标签和搅拌,以提高产量。我们实现了类似的质量和T7 RNA聚合酶的滴度超过4个数量级的反应量生产。这一原则证明,CFE是分散生物治疗生产的可行解决方案,可以加强对未来公共卫生危机或紧急威胁的准备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scalable Cell-Free Production of Active T7 RNA Polymerase

The SARS-CoV-2 pandemic highlighted the urgent need for biomanufacturing paradigms that are robust and fast. Here, we demonstrate the rapid process development and scalable cell-free production of T7 RNA polymerase, a critical component in mRNA vaccine synthesis. We carry out a 1-L cell-free gene expression (CFE) reaction that achieves over 90% purity, low endotoxin levels, and enhanced activity relative to commercial T7 RNA polymerase. To achieve this demonstration, we implement rolling circle amplification to circumvent difficulties in DNA template generation, and tune cell-free reaction conditions, such as temperature, additives, purification tags, and agitation, to boost yields. We achieve production of a similar quality and titer of T7 RNA polymerase over more than four orders of magnitude in reaction volume. This proof of principle positions CFE as a viable solution for decentralized biotherapeutic manufacturing, enhancing preparedness for future public health crises or emergent threats.

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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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