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Immunoprecipitation middle-up LC-MS for in vivo drug-to-antibody ratio determination for antibody-drug conjugates

机译:用于抗体 - 药物缀合物的体内药物对抗体比例的免疫沉淀中升LC-MS

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Aim: Drug-to-antibody ratio (DAR) determination is critical for development of antibody-drug conjugates (ADCs). This work presents a middle-up LC-MS approach for DAR analysis using prelabeled capture beads and in-house fabricated slit-plates. Methodology & Results: Cysteine, engineered cysteine and disulfide-linked ADCs, each with two different linker payloads, were immunocaptured and digested to scFc and F(ab')(2) fragments. At this point, disulfide-linked ADCs were analyzed while cysteine and engineered cysteine ADCs were reduced to LC and Fd' fragments for analysis. Results were precise, accurate and sensitive, allowing DAR to be determined out to 21 days. Conclusion: This work describes a method that is easily implemented, amenable to high-throughput analysis and does not require specialized reagents or equipment.
机译:目的:药物 - 抗体比(DAR)测定对于抗体 - 药物缀合物(ADC)的发展至关重要。 这项工作介绍了使用预订捕获珠和内部制造的狭缝的DAR分析的中间LC-MS方法。 方法和结果:半胱氨酸,工程半胱氨酸和二硫化物连接的ADC,各自具有两种不同的接头有效载荷,免疫缔造并消化为SCFC和F(AB')(2)片段。 此时,分析二硫化物连接的ADC,同时将半胱氨酸和工程化半胱氨酸ADC减少到LC和FD'片段进行分析。 结果精确,准确和敏感,允许DAR确定为21天。 结论:这项工作描述了一种易于实施的方法,适用于高通量分析,不需要专门的试剂或设备。

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