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Journal article

Ionic liquid-based strategy for predicting protein aggregation propensity and thermodynamic stability

Abstract:

Novel drug candidates are continuously being developed to combat the most life-threatening diseases; however, many promising protein therapeutics are dropped from the pipeline. During biological and industrial processes, protein therapeutics are exposed to various stresses such as fluctuations in temperature, solvent pH, and ionic strength. These can lead to enhanced protein aggregation propensity, one of the greatest challenges in drug development. Recently, ionic liquids (ILs), in particular, biocompatible choline chloride ([Cho]Cl)-based ILs, have been used to hinder stress-induced protein conformational changes. Herein, we develop an IL-based strategy to predict protein aggregation propensity and thermodynamic stability. We examine three key variables influencing protein misfolding: pH, ionic strength, and temperature. Using dynamic light scattering, zeta potential, and variable temperature circular dichroism measurements, we systematically evaluate the structural, thermal, and thermodynamic stability of fresh immunoglobin G4 (IgG4) antibody in water and 10, 30, and 50 wt % [Cho]Cl. Additionally, we conduct molecular dynamics simulations to examine IgG4 aggregation propensity in each system and the relative favorability of different [Cho]Cl-IgG4 packing interactions. We re-evaluate each system following 365 days of storage at 4 °C and demonstrate how to predict the thermodynamic properties and protein aggregation propensity over extended storage, even under stress conditions. We find that increasing [Cho]Cl concentration reduced IgG4 aggregation propensity both fresh and following 365 days of storage and demonstrate the potential of using our predictive IL-based strategy and formulations to radically increase protein stability and storage.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/jacsau.2c00356

Authors


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Role:
Author
ORCID:
0000-0002-0415-3050
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Institution:
University of Oxford
Division:
MPLS
Department:
Engineering Science
Oxford college:
Linacre College
Role:
Author
ORCID:
0000-0001-7215-9633
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Role:
Author
ORCID:
0000-0003-3431-2371


Publisher:
American Chemical Society
Journal:
JACS Au More from this journal
Volume:
2
Issue:
9
Pages:
2068–2080
Publication date:
2022-09-09
Acceptance date:
2022-08-18
DOI:
EISSN:
2691-3704
Pmid:
36186557


Language:
English
Keywords:
Pubs id:
1281897
Local pid:
pubs:1281897
Deposit date:
2023-02-24

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