Analytical Chemistry, Regeneron Pharmaceuticals Inc., 777 Old Saw Mill River Road, Tarrytown, New York 10591-6706, United States.
Anal Chem. 2024 Feb 6;96(5):1890-1897. doi: 10.1021/acs.analchem.3c03884. Epub 2024 Jan 23.
Despite substantial efforts to detect host cell proteins (HCPs) in antibody drugs, information regarding HCPs in gene therapy products remains limited and has not been widely integrated into the host cell engineering or purification processes. Most methods that have successfully detected HCPs in antibody drugs are not applicable to gene therapy products, except for the ProteoMiner enrichment method. Here, we demonstrate that ProteoMiner beads effectively enrich HCPs in adeno-associated virus (AAV) products and simultaneously remove the detergent Pluronic F-68 without a loss of low-abundance HCPs. Following optimization of this technique, there was up to a 34-fold increase in the enrichment of HCPs compared to direct digestion. Moreover, the detection limit was significantly lowered with the ability to detect HCPs at levels as low as 0.1 ng/mL after ProteoMiner treatment. This approach holds promise in AAV HCP analysis and may be adaptable to other gene therapy products. The findings from this study provide valuable insights into HCPs in AAV products and may facilitate process development and host cell line optimization. The high sensitivity of this approach also facilitates detection of critical low-abundance HCPs, thereby contributing to risk assessment of their impact on the safety and quality of the AAV-based gene therapy products.
尽管已经做出了大量努力来检测抗体药物中的宿主细胞蛋白 (HCP),但关于基因治疗产品中的 HCP 的信息仍然有限,并且尚未广泛整合到宿主细胞工程或纯化过程中。除了 ProteoMiner 富集方法外,大多数成功用于检测抗体药物中 HCP 的方法不适用于基因治疗产品。在这里,我们证明 ProteoMiner 珠粒可有效地富集腺相关病毒 (AAV) 产品中的 HCP,并同时去除去污剂 Pluronic F-68,而不会损失低丰度的 HCP。在对该技术进行优化后,与直接消化相比,HCP 的富集增加了多达 34 倍。此外,经过 ProteoMiner 处理后,检测限显著降低,能够检测到低至 0.1ng/mL 的 HCP。该方法在 AAV HCP 分析中具有广阔的应用前景,并且可能适用于其他基因治疗产品。本研究的结果为 AAV 产品中的 HCP 提供了有价值的见解,并可能有助于工艺开发和宿主细胞系优化。该方法的高灵敏度还促进了对关键低丰度 HCP 的检测,从而有助于评估它们对基于 AAV 的基因治疗产品安全性和质量的影响。