Monolithic Papain-Immobilized Enzyme Reactors for Automated Structural Characterization of Monoclonal Antibodies

Bibliographic Details
Title: Monolithic Papain-Immobilized Enzyme Reactors for Automated Structural Characterization of Monoclonal Antibodies
Authors: Francesca Rinaldi, Sara Tengattini, Gloria Brusotti, Giuseppe Tripodo, Benjamin Peters, Caterina Temporini, Gabriella Massolini, Enrica Calleri
Source: Frontiers in Molecular Biosciences, Vol 8 (2021)
Publisher Information: Frontiers Media S.A., 2021.
Publication Year: 2021
Collection: LCC:Biology (General)
Subject Terms: monoclonal antibodies, analytical characterization, immobilized enzyme reactor (IMER), monolithic supports, polymerized high internal phase emulsions (polyHIPEs), papain, Biology (General), QH301-705.5
More Details: The characterization of monoclonal antibodies (mAbs) requires laborious and time-consuming sample preparation steps before the liquid chromatography–mass spectrometry (LC-MS) analysis. Middle-up approaches entailing the use of specific proteases (papain, IdeS, etc.) emerged as practical and informative methods for mAb characterization. This work reports the development of immobilized enzyme reactors (IMERs) based on papain able to support mAb analytical characterization. Two monolithic IMERs were prepared by the covalent immobilization of papain on different supports, both functionalized via epoxy groups: a Chromolith® WP 300 Epoxy silica column from Merck KGaA and a polymerized high internal phase emulsion (polyHIPE) material synthesized by our research group. The two bioreactors were included in an in-flow system and characterized in terms of immobilization yield, kinetics, activity, and stability using Nα-benzoyl-L-arginine ethyl ester (BAEE) as a standard substrate. Moreover, the two bioreactors were tested toward a standard mAb, namely, rituximab (RTX). An on-line platform for mAb sample preparation and analysis with minimal operator manipulation was developed with both IMERs, allowing to reduce enzyme consumption and to improve repeatability compared to in-batch reactions. The site-specificity of papain was maintained after its immobilization on silica and polyHIPE monolithic supports, and the two IMERs were successfully applied to RTX digestion for its structural characterization by LC-MS. The main pros and cons of the two supports for the present application were described.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2296-889X
Relation: https://www.frontiersin.org/articles/10.3389/fmolb.2021.765683/full; https://doaj.org/toc/2296-889X
DOI: 10.3389/fmolb.2021.765683
Access URL: https://doaj.org/article/42c28a381a7749fe9825f9b785333003
Accession Number: edsdoj.42c28a381a7749fe9825f9b785333003
Database: Directory of Open Access Journals
More Details
ISSN:2296889X
DOI:10.3389/fmolb.2021.765683
Published in:Frontiers in Molecular Biosciences
Language:English