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DEVELOPING INTEGRATED PLATFORMS FOR THE GENERATION OF CELL LINES EXPRESSING BISPECIFIC PROTEINS WITH DESIRED QUALITIES

机译:开发用于产生表达具有所需质量双特异性蛋白质的细胞系的综合平台

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Complex bispecific and novel molecules are increasingly being developed as therapeutic proteins. These molecules present challenges for the generation of high quality manufacturing cell lines with good productivity and desirable product quality. High aggregation, poor sialylation and multiple chain mispairing are three of the major product quality problems affecting these molecules. To address these issues, we have developed a new expression platform which has been combined with high throughput analytical assays to screen and select clones with the preferred product quality profiles. Case studies will be presented on the development of cell lines expressing two types of bispecific molecules. To address the high level of aggregation observed with a bispecific molecule, the underlying cause of aggregation has been investigated and vector engineering tools have been applied to manipulate the expression of specific subunits of the protein leading to reduced aggregation. For another monomeric bispecific project, cell lines expressing four different polypeptides are generated and then efficiently screening at early stages of development to identify those with a high proportion of correctly assembled protein. These results also provide valuable information to assist in the molecular design and protein engineering of bispecific molecules.
机译:复杂的双特异性和新型分子正日益被开发为治疗性蛋白质。这些分子对于产生具有良好生产率和所需产品质量的高质量生产细胞系提出了挑战。高聚集,低唾液酸化和多链错配是影响这些分子的三个主要产品质量问题。为解决这些问题,我们开发了一个新的表达平台,该平台已与高通量分析检测相结合,以筛选和选择具有首选产品质量概况的克隆。将对表达两种类型的双特异性分子的细胞系的开发进行案例研究。为了解决用双特异性分子观察到的高水平的聚集,已经研究了聚集的根本原因,并且已经使用载体工程工具来操纵蛋白质的特定亚基的表达,从而导致聚集减少。对于另一个单体双特异性项目,将产生表达四种不同多肽的细胞系,然后在发育的早期阶段进行高效筛选,以鉴定出具有正确比例组装的蛋白质的高比例的细胞系。这些结果也提供了有价值的信息,以协助双特异性分子的分子设计和蛋白质工程。

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