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Investigating pH Effects on Enzymes Catalyzing Polysorbate Degradation by Activity-Based Protein Profiling
Alireza Dehghani1, Florian Binder1, Michael Zorn1
1Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Strasse 65, Biberach D-88397, Germany.
Host cell proteins (HCPs) can degrade biotherapeutic excipients like polysorbates. This study used activity-based protein profiling to identify pH-dependent HCP activity, revealing new carboxylesterase enzymes.
Area of Science:
- Biopharmaceutical manufacturing
- Protein chemistry
- Analytical chemistry
Background:
- Host cell proteins (HCPs) are critical impurities in biotherapeutics.
- Enzymatic activity of HCPs can degrade polysorbates (PS), impacting drug stability and shelf-life.
- Understanding HCP activity is vital for biopharmaceutical quality control.
Purpose of the Study:
- To investigate the impact of pH on the activity of HCPs capable of degrading polysorbates.
- To identify specific HCPs responsible for polysorbate degradation using activity-based protein profiling (ABPP).
- To evaluate the utility of different chemical probes for HCP activity profiling.
Main Methods:
- Activity-Based Protein Profiling (ABPP) was employed to profile HCP activity.
- Two distinct probes were used: a fluorophosphonate-Desthiobiotin probe and an Orlistat-based probe (OBP).
- Experiments were conducted across varying pH conditions to assess enzyme activity dependence.
Main Results:
- Over 50 HCPs were identified with significant pH-dependent enzymatic activity.
- The Orlistat-based probe (OBP) demonstrated broader coverage for identifying active HCPs compared to the FP probe.
- Three previously unreported active carboxylesterase family HCPs were discovered.
Conclusions:
- pH significantly influences HCP activity relevant to polysorbate degradation.
- Utilizing multiple ABPP probes, like OBP, enhances the comprehensive identification of active HCPs.
- This research provides crucial insights for mitigating HCP-related degradation in biotherapeutics.
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