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无消化的中间向下质谱法用于定量分析抗体药物偶联物中结合的有效载物

Digestion-Free Middle-Down Mass Spectrometry Method for Absolute Quantification of Conjugated Payload from Antibody-Drug Conjugates.

机构信息

Integrated Bioanalysis, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.

出版信息

Anal Chem. 2024 Oct 22;96(42):16475-16480. doi: 10.1021/acs.analchem.4c03383. Epub 2024 Sep 19.

Abstract

Antibody-drug conjugate (ADC) is a therapeutic modality that aims to improve payload delivery specificity and reduce systemic toxicity. Considering the complex structure of ADCs, various bioanalytical methods by liquid chromatography coupled with mass spectrometry (LC-MS), ligand binding assay (LBA) and hybrid LBA-LC-MS approaches have been established for ADC characterization and quantification. LCMS-based assays enable drug-antibody ratio (DAR) sensitive quantification of the conjugated payload. Typically, for quantitative, DAR-sensitive, assessment by LC-MS/MS,the conjugated payload is enzymatically liberated and quantified. Despite recent advances in ADC bioanalytical methods, the DAR-sensitive quantification of noncleavable linker ADCs by LC-MS/MS remains challenging. Thus, we developed a novel digestion-free middle-down mass spectrometry (DF-MDMS) using a collision-induced dissociation approach for absolute quantification of conjugated payload from four different ADCs in a biological matrix with minimum sample preparation. These results demonstrate that ADCs with different linker-payload structures can be quantified, including a noncleavable linker ADC, trastuzumab emtansine. It also shows that the assay sensitivity is comparable to the conventional ADC quantification method by linker-payload cleavage using enzyme, while the assay dynamic range depends on factors including payload ionization and dissociation efficiency, DAR and its distribution, and species abundance. By demonstrating absolute quantification of both cleavable and noncleavable linker ADCs, this novel middle-down ADC approach demonstrates its potential application in bioanalysis and analytical characterization, especially for early discovery where high-throughput screening is required as the new approach saves time and resources by not requiring enzymatic digestion for cleavable ADCs or development of anti-payload antibodies for noncleavable linker ADCs.

摘要

抗体药物偶联物 (ADC) 是一种治疗方式,旨在提高有效载荷的递送特异性并降低全身毒性。鉴于 ADC 的复杂结构,已经建立了各种基于液相色谱-质谱联用 (LC-MS)、配体结合测定法 (LBA) 和混合 LBA-LC-MS 方法的生物分析方法,用于 ADC 的表征和定量。基于 LCMS 的测定法能够对连接的有效载荷进行药物抗体比 (DAR) 敏感定量。通常,对于定量、DAR 敏感的 LC-MS/MS 评估,将连接的有效载荷酶促释放并定量。尽管 ADC 生物分析方法最近取得了进展,但通过 LC-MS/MS 对不可裂解连接子 ADC 进行 DAR 敏感定量仍然具有挑战性。因此,我们开发了一种新的无酶切中间向下质谱 (DF-MDMS) 方法,使用碰撞诱导解离方法,在最小样品制备的情况下,对生物基质中的四种不同 ADC 中的连接的有效载荷进行绝对定量。这些结果表明,可以对具有不同连接子-有效载荷结构的 ADC 进行定量,包括不可裂解的连接子 ADC 曲妥珠单抗-美坦新。它还表明,该测定的灵敏度与使用酶进行连接子-有效载荷切割的常规 ADC 定量方法相当,而测定的动态范围取决于包括有效载荷离子化和解离效率、DAR 及其分布以及物种丰度在内的因素。通过证明可裂解和不可裂解连接子 ADC 的绝对定量,这种新的中间向下 ADC 方法证明了其在生物分析和分析表征中的潜在应用,特别是在早期发现中,需要高通量筛选,因为新方法通过不要求对可裂解 ADC 进行酶切或开发针对不可裂解连接子 ADC 的抗有效载荷抗体,从而节省时间和资源。

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