Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1)
Selection of biophysically favorable antibody variants using a modified Flp-In CHO mammalian display platform
Julkaisun tekijät: Huhtinen Olli, Salbo Rune, Lamminmäki Urpo, Prince Stuart
Kustantaja: Frontiers Media S.A.
Julkaisuvuosi: 2023
Journal: Frontiers in Bioengineering and Biotechnology
Tietokannassa oleva lehden nimi: Frontiers in bioengineering and biotechnology
Lehden akronyymi: Front Bioeng Biotechnol
Artikkelin numero: 1170081
Volyymi: 11
ISSN: 2296-4185
eISSN: 2296-4185
DOI: http://dx.doi.org/10.3389/fbioe.2023.1170081
Verkko-osoite: https://www.frontiersin.org/articles/10.3389/fbioe.2023.1170081/full
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/179638161
Mammalian display enables the selection of biophysically favorable antibodies from a large IgG antibody library displayed on the plasma membrane of mammalian cells. We constructed and validated a novel mammalian display platform utilizing the commercially available Flp-In CHO cell line as a starting point. We introduced a single copy of a landing pad for Bxb1 integrase-driven recombinase-mediated cassette exchange into the FRT site of the Flp-In CHO line to facilitate the efficient single-copy integration of an antibody display cassette into the genome of the cell line. We then proceeded to demonstrate the ability of our platform to select biophysically favorable antibodies from a library of 1 × 106 displayed antibodies designed to improve the biophysical properties of bococizumab via randomization of problematic hydrophobic surface residues of the antibody. Enrichment of bococizumab variants via fluorescence-activated cell sorting selections was followed by next generation sequencing and thorough characterization of biophysical properties of 10 bococizumab variants that subsequently allowed attribution of the mutations to the biophysical properties of the antibody variants. The mammalian displayed variants exhibited reduced aggregation propensity and polyreactivity, while critically retaining its target binding thereby demonstrating the utility of this valuable tool.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
