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A protein‐stabilizing technology for enhanced antibody stability and antibody‐binding profiles in a microchip array
Author(s) -
Scholz Martin,
Lüking Angelika
Publication year - 2012
Publication title -
biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.144
H-Index - 84
eISSN - 1860-7314
pISSN - 1860-6768
DOI - 10.1002/biot.201100494
Subject(s) - antibody , adalimumab , recombinant dna , chemistry , monoclonal antibody , antibody microarray , protein microarray , antigen , computational biology , microarray , microbiology and biotechnology , biology , biochemistry , immunology , tumor necrosis factor alpha , gene expression , gene
The stability of therapeutic antibodies during downstream processing and storage is important for functionality and quality. To determine functional antibody performance, the UNIchip ® high‐density protein microarray with 384 recombinant antigenic targets was developed; this allows characterization of antibody specificity by generating standardized quantitative binding profiles. In this study, we used UNIchip ® to test the efficacy of a novel protein stabilizing and protecting solution (SPS) to preserve the binding specificity and binding strength of a therapeutic anti‐TNF‐α antibody (Adalimumab; Humira). Our results show that reconstituted SPS‐formulated and lyophilized Adalimumab elicits significantly less off‐target activity after reconstitution and preserves binding strength even after six weeks of storage at 40°C compared with Adalimumab that underwent the same treatment with the original formulation. By means of UNIchip ® , we were able to confirm the protein stabilizing effects of SPS as shown by preserved antibody functionality.

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