Praesto Jetted A50 HipH是一种温和pH值的蛋白a洗脱树脂,具有更好的聚集体分离能力,并且对流动相添加剂氯化钠的蛋白洗脱具有独特的响应。

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Wenwen Lu, Yan Wan, Yifeng Li
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引用次数: 0

摘要

蛋白A亲和层析法已广泛应用于单克隆抗体(mAb)、双特异性抗体(bsAb)和fc融合蛋白的纯化。然而,洗脱所需的低pH值(即3.0-3.5)可能导致pH敏感分子聚集和/或截断。来自Purolite的Praesto Jetted A50 HipH是一种新推出的Protein a树脂,其配体经过设计,可以在较温和的pH(即4.6或更高)下进行抗体/ fc融合洗脱,因此更适合pH敏感分子。在目前的研究中,我们证明了这种新的蛋白A树脂除了可以温和洗脱外,与传统的蛋白A树脂相比,还具有更好的聚集体分离能力。传统的蛋白A树脂通常缺乏任何团聚体分离能力,而Jetted A50 HipH可以去除负载中高达70%的团聚体,同时保持良好的单体回收率。此外,我们发现Jetted A50 HipH柱的蛋白洗脱对流动相添加剂氯化钠的反应与传统蛋白A柱不同(洗脱被促进而不是抑制)。当在洗脱缓冲液中加入适量的氯化钠时,该特性可以在进一步增加的pH(即5)下进行洗脱。因此,Jetted A50 HipH是比传统的蛋白a树脂更好的选择,用于ph敏感和/或聚集倾向的单抗、bsab和fc融合蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Praesto Jetted A50 HipH, a mild pH elution protein A resin, exhibits improved aggregate separation capability and protein elution from it shows unique response to mobile phase additive sodium chloride
Protein A affinity chromatography has been widely used for product capture in monoclonal antibody (mAb), bispecific antibody (bsAb) and Fc-fusion protein purification. However, the low pH (i.e., 3.0–3.5) required for elution may cause aggregation and/or truncation for pH-sensitive molecules. Praesto Jetted A50 HipH from Purolite is a newly launched Protein A resin whose ligand is engineered to enable antibody/Fc-fusion elution at a milder pH (i.e., 4.6 or above) and therefore is more suitable to pH-sensitive molecules. In the current study, we demonstrated that this new Protein A resin, besides allowing mild elution, also possesses improved aggregate separation capability in comparison to traditional Protein A resins. While traditional Protein A resins generally lack any aggregate separation capability, Jetted A50 HipH can remove up to 70% of the aggregates in the load while maintaining good monomer recovery. In addition, we discovered that protein elution from Jetted A50 HipH column responded to mobile phase additive sodium chloride differently from that from traditional Protein A columns (elution was promoted rather than suppressed). This property enables elution at further increased pH (i.e., 5) when proper amount of sodium chloride is included in the elution buffer. Thus, Jetted A50 HipH is a better choice than traditional Protein A resins for pH-sensitive and/or aggregation-prone mAbs, bsAbs and Fc-fusion proteins.
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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.
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