信使核糖核酸
计算生物学
核糖核酸
计算机科学
质量(理念)
生物
基因
遗传学
物理
量子力学
作者
Helen M. Gunter,Senel Idrisoglu,Abhishek Singh,Dae Jong Han,Emily Ariens,Jonathan R. Peters,Ted Wong,Seth W. Cheetham,Jun Xu,Subash Rai,Robert Feldman,Andrew P. Herbert,Esteban Marcellin,Romain Tropée,Trent P. Munro,Tim R. Mercer
标识
DOI:10.1038/s41467-023-41354-y
摘要
Abstract The success of mRNA vaccines has been realised, in part, by advances in manufacturing that enabled billions of doses to be produced at sufficient quality and safety. However, mRNA vaccines must be rigorously analysed to measure their integrity and detect contaminants that reduce their effectiveness and induce side-effects. Currently, mRNA vaccines and therapies are analysed using a range of time-consuming and costly methods. Here we describe a streamlined method to analyse mRNA vaccines and therapies using long-read nanopore sequencing. Compared to other industry-standard techniques, VAX-seq can comprehensively measure key mRNA vaccine quality attributes, including sequence, length, integrity, and purity. We also show how direct RNA sequencing can analyse mRNA chemistry, including the detection of nucleoside modifications. To support this approach, we provide supporting software to automatically report on mRNA and plasmid template quality and integrity. Given these advantages, we anticipate that RNA sequencing methods, such as VAX-seq, will become central to the development and manufacture of mRNA drugs.
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