Evidence map›Paper›PMID 39031865›Full record

ArticleBiotechnology journal2024

Expanding the RNA polymerase biocatalyst solution space for mRNA manufacture.

Edward Curry, Svetlana Sedelnikova, John Rafferty, Martyn Hulley, Melinda Pohle, George Muir, Adam Brown

Abstract read
In one paragraph

Article in Biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Cold-adapted RNA polymerase fromProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Edward CurryDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield, UK.ORCID https://orcid.org/0000-0002-5123-8866
Svetlana SedelnikovaSchool of Biosciences, University of Sheffield, Sheffield, UK.
John RaffertySchool of Biosciences, University of Sheffield, Sheffield, UK.
Martyn HulleyBioprocess Development, AstraZeneca, Cambridge, UK.
Melinda PohleDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield, UK.
George MuirDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield, UK.
Adam BrownDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield, UK.

Funding

AstraZenecaBiotechnology and Biological Sciences Research Council BB/T508664/1
6 · The paper itself

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.

Indexed as

DNA-Directed RNA PolymerasesRNA, MessengerBiocatalysisEscherichia coliRecombinant ProteinsTranscription, GeneticDNA-Directed RNA PolymerasesRecombinant ProteinsRNA, Messengercell‐free screeningin vitro transcriptionmRNA manufactureRNA polymerase

Identifiers

PMID39031865
PMCPMC11475235

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.