Expanding the RNA polymerase biocatalyst solution space for mRNA manufacture

IF 3.2 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Biotechnology Journal Pub Date : 2024-06-21 DOI:10.1002/biot.202400012
Edward Curry, Svetlana Sedelnikova, John Rafferty, Martyn Hulley, Melinda Pohle, George Muir, Adam Brown
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Abstract

All mRNA products are currently manufactured in in vitro transcription (IVT) reactions that utilize single-subunit RNA polymerase (RNAP) biocatalysts. Although it is known that discrete polymerases exhibit highly variable bioproduction phenotypes, including different relative processivity rates and impurity generation profiles, only a handful of enzymes are generally available for mRNA biosynthesis. This limited RNAP toolbox restricts strategies to design and troubleshoot new mRNA manufacturing processes, which is particularly undesirable given the continuing diversification of mRNA product lines toward larger and more complex molecules. Herein, we describe development of a high-throughput RNAP screening platform, comprising complementary in silico and in vitro testing modules, that enables functional characterization of large enzyme libraries. Utilizing this system, we identified eight novel sequence-diverse RNAPs, with associated active cognate promoters, and subsequently validated their performance as recombinant enzymes in IVT-based mRNA production processes. By increasing the number of available characterized functional RNAPs by more than 130% and providing a platform to rapidly identify further potentially useful enzymes, this work significantly expands the RNAP biocatalyst solution space for mRNA manufacture, thereby enhancing the capability for application-specific and molecule-specific optimization of both product yield and quality.

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为 mRNA 生产拓展 RNA 聚合酶生物催化剂解决方案空间
目前,所有 mRNA 产品都是在体外转录(IVT)反应中利用单亚基 RNA 聚合酶(RNAP)生物催化剂制造的。虽然众所周知,不同的聚合酶表现出高度可变的生物生产表型,包括不同的相对加工率和杂质生成情况,但一般只有少数几种酶可用于 mRNA 生物合成。这种有限的 RNAP 工具箱限制了设计新 mRNA 制造工艺和排除故障的策略,鉴于 mRNA 产品线不断向更大和更复杂的分子方向发展,这种限制尤其不可取。在本文中,我们介绍了高通量 RNAP 筛选平台的开发情况,该平台由互补的硅学和体外测试模块组成,可对大型酶库进行功能表征。利用该系统,我们确定了 8 种新型序列多样的 RNAP 及其相关的活性同源启动子,并随后验证了它们在基于 IVT 的 mRNA 生产过程中作为重组酶的性能。通过将可用的特征功能 RNAP 数量增加 130% 以上,并提供一个快速鉴定更多潜在有用酶的平台,这项工作极大地扩展了用于 mRNA 生产的 RNAP 生物催化剂解决方案空间,从而提高了针对特定应用和特定分子优化产品产量和质量的能力。
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来源期刊
Biotechnology Journal
Biotechnology Journal Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
2.10%
发文量
123
审稿时长
1.5 months
期刊介绍: Biotechnology Journal (2019 Journal Citation Reports: 3.543) is fully comprehensive in its scope and publishes strictly peer-reviewed papers covering novel aspects and methods in all areas of biotechnology. Some issues are devoted to a special topic, providing the latest information on the most crucial areas of research and technological advances. In addition to these special issues, the journal welcomes unsolicited submissions for primary research articles, such as Research Articles, Rapid Communications and Biotech Methods. BTJ also welcomes proposals of Review Articles - please send in a brief outline of the article and the senior author''s CV to the editorial office. BTJ promotes a special emphasis on: Systems Biotechnology Synthetic Biology and Metabolic Engineering Nanobiotechnology and Biomaterials Tissue engineering, Regenerative Medicine and Stem cells Gene Editing, Gene therapy and Immunotherapy Omics technologies Industrial Biotechnology, Biopharmaceuticals and Biocatalysis Bioprocess engineering and Downstream processing Plant Biotechnology Biosafety, Biotech Ethics, Science Communication Methods and Advances.
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