还原(数学)
半胱氨酸
单体
分布(数学)
共价键
组合化学
化学
生物化学
色谱法
数学
酶
有机化学
几何学
数学分析
聚合物
作者
Elsa Wagner‐Rousset,Olivier Colas,Yannis-Nicolas François,Sabine Heinisch,Davy Guillarme,Sarah Cianférani,Alain Beck
标识
DOI:10.1007/978-1-4939-9929-3_12
摘要
High-resolution native mass spectrometry (MS) provides accurate mass measurements (within 30 ppm) of intact ADCs and can also yield drug load distribution (DLD) and average drug to antibody ratio (DAR) in parallel with hydrophobic interaction chromatography (HIC). Native MS is furthermore unique in its ability to simultaneously detect covalent and noncovalent species in a mixture and for HIC peak identity assessment offline or online.
As an orthogonal method described in this chapter, LC-MS following ADC reduction or IdeS (Fabricator) digestion and reduction can also be used to measure the DLD of light chain and Fd fragments for hinge native cysteine residues such as brentuximab vedotin. Both methods allow also the measurement of average DAR for both monomeric and multimeric species. In addition, the Fc fragments can be analyzed in the same run, providing a complete glycoprofile and the demonstration or absence of additional conjugation of this subdomain involved in FcRn and Fc-gammaR binding.
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