Growth of Clusters toward Liquid–Liquid Phase Separation of Monoclonal Antibodies as Characterized by Small-Angle X-ray Scattering and Molecular Dynamics Simulation

In concentrated protein solutions, short-range attractions (SRAs) contribute to liquid-liquid phase separation (LLPS) as a function of temperature and salinity, particularly when the charge and thus long-range repulsions are low near the isoelectric point pI. Herein, we study how SRA and solution morphology vary with the approach to LLPS from increased SRA for two monoclonal antibodies (mAbs) as salt concentration is reduced near the pI. These properties are quantified using small-angle X-ray scattering (SAXS) interpreted via coarse-grained (CG) molecular dynamics (MD) simulations and compared with less descriptive properties from static and dynamic light scattering. Experimental structure factors are fit with a library of MD simulations for a CG 12-bead mAb model to determine the SRA strength (<i>K</i>) and cluster size distributions. Proximity to LLPS and clustering characteristics in mAb solutions are impacted by both net charge, which are modified by pH, and the strength of anisotropic electrostatic SRA (charge-charge, charge-dipole, hydrogen bonding, etc.), which are screened and weakened by added salts. The trends in LLPS are consistent with the reduced diffusion interaction parameter kD<i>/B</i><sub>22</sub><sup>ex</sup> for dilute solutions. However, greater insight is provided with SAXS along with CG-MD simulations; in particular, the growth of clusters is observed with the approach to LLPS with decreasing salinity over a wide range of concentrations.

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Publication Details

Journal
The Journal of Physical Chemistry B
Published
2025-03-07
DOI
https://doi.org/10.1021/acs.jpcb.4c07064
Citations
5
Primary Topic
Protein purification and stability
Type
article
Field-Weighted Citation Impact
4.03

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article

Growth of Clusters toward Liquid–Liquid Phase Separation of Monoclonal Antibodies as Characterized by Small-Angle X-ray Scattering and Molecular Dynamics Simulation

Jintian Huang, Ranajoy Majumdar, Marta A. Witek, Alfredo Lanzaro et al.
5 citations
The Journal of Physical Chemistry B
Protein purification and stability
4.03
article

Growth of Clusters toward Liquid–Liquid Phase Separation of Monoclonal Antibodies as Characterized by Small-Angle X-ray Scattering and Molecular Dynamics Simulation

Jintian Huang, Ranajoy Majumdar, Marta A. Witek, Alfredo Lanzaro, Ken K. Qian, Alexander E. Marras, Mahlet A. Woldeyes, Jiangyan Feng, J. Lewandowski, Richard E. Gillilan, Thomas M. Truskett, Qingqiu Huang, Keith P. Johnston, William D. Kimball, C. M. Hurd, Neel Jhaveri
article en
5 citations

Abstract

In concentrated protein solutions, short-range attractions (SRAs) contribute to liquid-liquid phase separation (LLPS) as a function of temperature and salinity, particularly when the charge and thus long-range repulsions are low near the isoelectric point pI. Herein, we study how SRA and solution morphology vary with the approach to LLPS from increased SRA for two monoclonal antibodies (mAbs) as salt concentration is reduced near the pI. These properties are quantified using small-angle X-ray scattering (SAXS) interpreted via coarse-grained (CG) molecular dynamics (MD) simulations and compared with less descriptive properties from static and dynamic light scattering. Experimental structure factors are fit with a library of MD simulations for a CG 12-bead mAb model to determine the SRA strength (<i>K</i>) and cluster size distributions. Proximity to LLPS and clustering characteristics in mAb solutions are impacted by both net charge, which are modified by pH, and the strength of anisotropic electrostatic SRA (charge-charge, charge-dipole, hydrogen bonding, etc.), which are screened and weakened by added salts. The trends in LLPS are consistent with the reduced diffusion interaction parameter kD<i>/B</i><sub>22</sub><sup>ex</sup> for dilute solutions. However, greater insight is provided with SAXS along with CG-MD simulations; in particular, the growth of clusters is observed with the approach to LLPS with decreasing salinity over a wide range of concentrations.

The Journal of Physical Chemistry BVol. 129(11)
Eli Lilly (United States) (US), Cornell University (US), Centre for Health Equity Studies (SE), Walker (United States) (US), The University of Texas at Austin (US)
Welch Foundation, Eli Lilly and Company, Division of Materials Research
Openalex Percentile: Top 7%
Protein purification and stability
4.03
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