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用于一步法纯化过程的多功能基于亲和力的系统的开发:以 A 组链球菌疫苗为例。

Development of versatile affinity-based system for one step purification process: Case of Group A Streptococcus vaccine.

机构信息

Affilogic, Nantes, France.

GSK, Siena, Italy.

出版信息

Biotechnol Bioeng. 2022 Nov;119(11):3210-3220. doi: 10.1002/bit.28199. Epub 2022 Aug 13.

DOI:10.1002/bit.28199
PMID:35906818
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9804325/
Abstract

Affinity capture is one of the most attractive strategies for simplifying downstream processing. Although it is a key mainstream approach for antibody purification, the same is not true for other biologics such as vaccines, mainly due to the lack of suitable affinity material. In this study, a novel custom affinity system is introduced permitting widespread adoption of affinity capture for the purification of biologics beyond antibodies. This is illustrated here by the development of a one-step purification process of a mutant form of streptolysin O (SLO), a vaccine candidate against Streptococcus pyogenes infection. The system consists of the association of custom ligands based on the Nanofitin protein scaffold, with Eshmuno® industry-grade chromatography medium. The Nanofitins were selected for their specificity to the target product. The newly developed affinity medium was used at different column sizes to monitor scalability from process development (1 ml) and robustness verification (5 ml) to pilot (133 ml) and technical (469 ml) runs. The single-step affinity purification consistently delivered high purity product (above > 90%) and improved performances compared with the current three-step process: reduced process time and footprint (3 to 1 step) and increased product yields (0.31 g vs. 0.04 g of SLO per kg of harvest broth). The custom affinity system herein described can potentially be applied to any biologic for which a specific Nanofitin is identified, thus establishing a platform with a strong impact on the manufacturing of vaccines and other biological targets.

摘要

亲和捕获是简化下游处理的最具吸引力的策略之一。尽管它是抗体纯化的关键主流方法,但对于其他生物制剂(如疫苗)并非如此,主要是因为缺乏合适的亲和材料。在本研究中,引入了一种新型定制亲和系统,允许广泛采用亲和捕获方法来纯化抗体以外的生物制剂。这里通过开发一种一步法纯化突变形式的链激酶 O(SLO)的过程来说明这一点,SLO 是一种针对化脓性链球菌感染的疫苗候选物。该系统由基于 Nanofitin 蛋白支架的定制配体的结合组成,与 Eshmuno®工业级色谱介质结合。选择 Nanofitins 是因为它们对目标产物具有特异性。新开发的亲和介质在不同的柱尺寸下使用,以监测从工艺开发(1ml)和稳健性验证(5ml)到中试(133ml)和技术(469ml)运行的可扩展性。一步亲和纯化始终提供高纯度产品(>90%),与当前的三步工艺相比,性能得到改善:减少工艺时间和占地面积(3 步减少到 1 步),提高产品收率(每公斤收获液的 SLO 产量从 0.04g 增加到 0.31g)。本文所述的定制亲和系统有可能适用于任何已鉴定出特定 Nanofitin 的生物制剂,从而建立一个对疫苗和其他生物靶标制造具有强大影响的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/0a0f4075d9c2/BIT-119-3210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/a6b79f8d1075/BIT-119-3210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/33b97660834d/BIT-119-3210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/40edb0d0e502/BIT-119-3210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/49bc74da1e8e/BIT-119-3210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/0a0f4075d9c2/BIT-119-3210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/a6b79f8d1075/BIT-119-3210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/33b97660834d/BIT-119-3210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/40edb0d0e502/BIT-119-3210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/49bc74da1e8e/BIT-119-3210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723e/9804325/0a0f4075d9c2/BIT-119-3210-g002.jpg

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Mol Cancer Ther. 2023 Nov 1;22(11):1343-1351. doi: 10.1158/1535-7163.MCT-22-0805.
4
Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents.用亲和功能化纳米纤维吸附剂高效捕获腺相关病毒血清型5
Front Bioeng Biotechnol. 2023 May 16;11:1183974. doi: 10.3389/fbioe.2023.1183974. eCollection 2023.
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4
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5
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