Fast and robust recombinant protein production utilizing episomal stable pools in WAVE bioreactors

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Melanie Dannemeyer, Anna Berling, Sara Kanje, Henric Enstedt, LanLan Xu, Delaram Afshari, Malin Westin, Gabriella Hober, Mathias Uhlén, Sophia Hober, Hanna Tegel
{"title":"Fast and robust recombinant protein production utilizing episomal stable pools in WAVE bioreactors","authors":"Melanie Dannemeyer,&nbsp;Anna Berling,&nbsp;Sara Kanje,&nbsp;Henric Enstedt,&nbsp;LanLan Xu,&nbsp;Delaram Afshari,&nbsp;Malin Westin,&nbsp;Gabriella Hober,&nbsp;Mathias Uhlén,&nbsp;Sophia Hober,&nbsp;Hanna Tegel","doi":"10.1016/j.pep.2024.106505","DOIUrl":null,"url":null,"abstract":"<div><p>Protein reagents are essential resources for several stages of drug discovery projects from structural biology and assay development through lead optimization. Depending on the aim of the project different amounts of pure protein are required. Small-scale expressions are initially used to determine the reachable levels of production and quality before scaling up protein reagent supply. Commonly, amounts of several hundreds of milligrams to grams are needed for different experiments, including structural investigations and activity evaluations, which require rather large cultivation volumes. This implies that cultivation of large volumes of either transiently transfected cells or stable pools/stable cell lines is needed. Hence, a production process that is scalable, speeds up the development projects, and increases the robustness of protein reagent quality throughout scales. Here we present a protein production pipeline with high scalability. We show that our protocols for protein production in Chinese hamster ovary cells allow for a seamless and efficient scale-up with robust product quality and high performance. The flexible scale of the production process, as shown here, allows for shorter lead times in drug discovery projects where there is a reagent demand for a specific protein or a set of target proteins.</p></div>","PeriodicalId":20757,"journal":{"name":"Protein expression and purification","volume":"221 ","pages":"Article 106505"},"PeriodicalIF":1.4000,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1046592824000779/pdfft?md5=9c8b668160a3752d0db74721d52fe3ff&pid=1-s2.0-S1046592824000779-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Protein expression and purification","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1046592824000779","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Protein reagents are essential resources for several stages of drug discovery projects from structural biology and assay development through lead optimization. Depending on the aim of the project different amounts of pure protein are required. Small-scale expressions are initially used to determine the reachable levels of production and quality before scaling up protein reagent supply. Commonly, amounts of several hundreds of milligrams to grams are needed for different experiments, including structural investigations and activity evaluations, which require rather large cultivation volumes. This implies that cultivation of large volumes of either transiently transfected cells or stable pools/stable cell lines is needed. Hence, a production process that is scalable, speeds up the development projects, and increases the robustness of protein reagent quality throughout scales. Here we present a protein production pipeline with high scalability. We show that our protocols for protein production in Chinese hamster ovary cells allow for a seamless and efficient scale-up with robust product quality and high performance. The flexible scale of the production process, as shown here, allows for shorter lead times in drug discovery projects where there is a reagent demand for a specific protein or a set of target proteins.

在 WAVE 生物反应器中利用外显子稳定池快速、稳健地生产重组蛋白。
蛋白质试剂是药物发现项目从结构生物学和检测开发到先导优化等多个阶段的重要资源。根据项目目标的不同,需要不同数量的纯蛋白。在扩大蛋白质试剂供应规模之前,最初使用小规模表达来确定可达到的产量和质量水平。不同的实验,包括结构研究和活性评估,通常需要几百毫克到几克的量,这就需要相当大的培养量。这意味着需要培养大量的瞬时转染细胞或稳定池/稳定细胞系。因此,需要一种可扩展的生产流程,以加快开发项目的速度,并提高蛋白质试剂质量的稳定性。在这里,我们提出了一种具有高度可扩展性的蛋白质生产流水线。我们的研究表明,我们在中国仓鼠卵巢细胞中生产蛋白质的方案可实现无缝、高效的规模化生产,并具有稳健的产品质量和高性能。如本文所示,灵活的生产工艺规模可以缩短药物发现项目中对特定蛋白质或一组目标蛋白质试剂的需求周期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Protein expression and purification
Protein expression and purification 生物-生化研究方法
CiteScore
3.70
自引率
6.20%
发文量
120
审稿时长
32 days
期刊介绍: Protein Expression and Purification is an international journal providing a forum for the dissemination of new information on protein expression, extraction, purification, characterization, and/or applications using conventional biochemical and/or modern molecular biological approaches and methods, which are of broad interest to the field. The journal does not typically publish repetitive examples of protein expression and purification involving standard, well-established, methods. However, exceptions might include studies on important and/or difficult to express and/or purify proteins and/or studies that include extensive protein characterization, which provide new, previously unpublished information.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信