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双特异性抗体下游纯化的当前趋势与挑战

Current trends and challenges in the downstream purification of bispecific antibodies.

作者信息

Chen Serene W, Zhang Wei

机构信息

Downstream Processing Group, Bioprocessing Technology Institute, Agency for Science, Technology and Research, Singapore 138668, Singapore.

出版信息

Antib Ther. 2021 May 7;4(2):73-88. doi: 10.1093/abt/tbab007. eCollection 2021 Apr.

Abstract

Bispecific antibodies (bsAbs) represent a highly promising class of biotherapeutic modality. The downstream processing of this class of antibodies is therefore of crucial importance in ensuring that these products can be obtained with high purity and yield. Due to the various fundamental structural similarities between bsAbs and monoclonal antibodies (mAbs), many of the current bsAb downstream purification methodologies are based on the established purification processes of mAbs, where affinity, charge, size, hydrophobicity and mixed-mode-based purification are frequently employed. Nevertheless, the downstream processing of bsAbs presents a unique set of challenges due to the presence of bsAb-specific byproducts, such as mispaired products, undesired fragments and higher levels of aggregates, that are otherwise absent or present in lower levels in mAb cell culture supernatants, thus often requiring the design of additional purification strategies in order to obtain products of high purity. Here, we outline the current major purification methods of bsAbs, highlighting the corresponding solutions that have been proposed to circumvent the unique challenges presented by this class of antibodies, including differential affinity chromatography, sequential affinity chromatography and the use of salt additives and pH gradients or multistep elutions in various modes of purification. Finally, a perspective towards future process development is offered.

摘要

双特异性抗体(bsAbs)是一类极具前景的生物治疗药物。因此,这类抗体的下游加工对于确保能够以高纯度和高产量获得这些产品至关重要。由于双特异性抗体与单克隆抗体(mAbs)之间存在各种基本结构相似性,当前许多双特异性抗体下游纯化方法都基于已确立的单克隆抗体制备工艺,其中经常采用基于亲和力、电荷、大小、疏水性和混合模式的纯化方法。然而,双特异性抗体的下游加工面临着一系列独特的挑战,因为存在双特异性抗体特有的副产物,如错配产物、不需要的片段和更高水平的聚集体,而这些在单克隆抗体细胞培养上清液中要么不存在,要么含量较低,因此通常需要设计额外的纯化策略以获得高纯度产品。在此,我们概述了当前双特异性抗体的主要纯化方法,重点介绍了为应对这类抗体所带来的独特挑战而提出的相应解决方案,包括差异亲和色谱法、顺序亲和色谱法以及在各种纯化模式中使用盐添加剂、pH梯度或多步洗脱。最后,对未来工艺开发进行了展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf34/8155696/5c40ca4d9712/tbab007f1.jpg

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