Methionine oxidation is among the most frequently observed post-translational modifications of monoclonal antibody (mAb) products during their manufacturing that can affect the drug’s safety and efficacy. Such modifications are typically assessed using bottom-up peptide mapping techniques. However, this methodology is often tedious and prone to generation of artefacts through sample preparation process. In this study, we present a middle-down method that is complementary to a bottom-up approach to characterise methionine oxidation in mAbs, utilising electron activated dissociation (EAD) on a ZenoTOF7600 (Sciex).
Oxidised and non-oxidised mAb samples were mixed to create different oxidation levels. These samples were digested to subunits (Lc, Fd’ and Fc/2) with IdeS protease and EndoS (for Fc/2 deglycosylation), denatured and then reduced. The samples were injected on to a Waters Acquity BEH C4 column and separated with a gradient elution of 0.1% FA in H2O and 0.1% FA in ACN at 7 µL/min. MS analysis was carried out using an optimised MRMHR EAD experiment on ZenoTOF7600. Data obtained were processed for subunit mass analysis, sequencing, oxidation identification and quantification using Sciex OS and Biologics Explorer software packages.
The optimised middle-down EAD method allowed us to measure different oxidised species of antibody subunits with 15 ppm or better mass accuracy. The MS/SM spectra showed the fragments mass shifts due to various oxidation on the subunits. EAD fragmentation allowed site-specific identification of methionine oxidation sites on Lc at M4; Fd’ at M34 and M101; Fc/2 at M16, M122 and M192. Quantification of oxidised mAb, using Fc/2, was achieved down to 1% oxidation level with a strong correlation (R2 > 0.99) between expected and measured oxidation percentage using both MS1 and MS2 quantification approaches.
A middle-down EAD method has been developed that can be applied for complimentary characterisation of site-specific methionine oxidation of mAb products during formulation process.