Literature DB >> 29045869

Metastability Gap in the Phase Diagram of Monoclonal IgG Antibody.

Jacob B Rowe1, Rachel A Cancel1, Tyler D Evangelous1, Rhiannon P Flynn1, Sergei Pechenov2, J Anand Subramony2, Jifeng Zhang3, Ying Wang4.   

Abstract

Crystallization of IgG antibodies has important applications in the fields of structural biology, biotechnology, and biopharmaceutics. However, a rational approach to crystallize antibodies is still lacking. In this work, we report a method to estimate the solubility of antibodies at various temperatures. We experimentally determined the full phase diagram of an IgG antibody. Using the full diagram, we examined the metastability gaps, i.e., the distance between the crystal solubility line and the liquid-liquid coexistence curve, of IgG antibodies. By comparing our results to the partial phase diagrams of other IgGs reported in literature, we found that IgG antibodies have similar metastability gaps. Thereby, we present an equation with two phenomenological parameters to predict the approximate location of the solubility line of IgG antibodies with respect to their liquid-liquid coexistence curves. We have previously shown that the coexistence curve of an antibody solution can be readily determined by the polyethylene glycol-induced liquid-liquid phase separation method. Combining the polyethylene glycol-induced liquid-liquid phase separation measurements and the phenomenological equation in this article, we provide a general and practical means to predict the thermodynamic conditions for crystallizing IgG antibodies in the solution environments of interest.
Copyright © 2017 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 29045869      PMCID: PMC5647622          DOI: 10.1016/j.bpj.2017.08.048

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  31 in total

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Journal:  Phys Rev Lett       Date:  1996-12-02       Impact factor: 9.161

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Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2002-03-01

3.  Crystalline and amorphous insulin-zinc compounds with prolonged action.

Authors:  K Hallas-Møller; K Petersen; J Schlichtkrull
Journal:  Science       Date:  1952-10-10       Impact factor: 47.728

4.  Crystallization mechanisms of hemoglobin C in the R state.

Authors:  Angela R Feeling-Taylor; S-T Yau; Dimiter N Petsev; Ronald L Nagel; Rhoda Elison Hirsch; Peter G Vekilov
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

Review 5.  Strategies and challenges for the next generation of therapeutic antibodies.

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6.  Binary-liquid phase separation of lens protein solutions.

Authors:  M L Broide; C R Berland; J Pande; O O Ogun; G B Benedek
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

7.  Effect of Hierarchical Cluster Formation on the Viscosity of Concentrated Monoclonal Antibody Formulations Studied by Neutron Scattering.

Authors:  P Douglas Godfrin; Isidro E Zarraga; Jonathan Zarzar; Lionel Porcar; Peter Falus; Norman J Wagner; Yun Liu
Journal:  J Phys Chem B       Date:  2016-01-07       Impact factor: 2.991

8.  Phase transitions in human IgG solutions.

Authors:  Ying Wang; Aleksey Lomakin; Ramil F Latypov; Jacob P Laubach; Teru Hideshima; Paul G Richardson; Nikhil C Munshi; Kenneth C Anderson; George B Benedek
Journal:  J Chem Phys       Date:  2013-09-28       Impact factor: 3.488

9.  Phase separation in solutions of monoclonal antibodies and the effect of human serum albumin.

Authors:  Ying Wang; Aleksey Lomakin; Ramil F Latypov; George B Benedek
Journal:  Proc Natl Acad Sci U S A       Date:  2011-09-15       Impact factor: 11.205

10.  The phase behavior study of human antibody solution using multi-scale modeling.

Authors:  Gang Sun; Ying Wang; Aleksey Lomakin; George B Benedek; H Eugene Stanley; Limei Xu; Sergey V Buldyrev
Journal:  J Chem Phys       Date:  2016-11-21       Impact factor: 3.488

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Journal:  MAbs       Date:  2018-12-17       Impact factor: 5.857

2.  Modeling the depletion effect caused by an addition of polymer to monoclonal antibody solutions.

Authors:  Yu V Kalyuzhnyi; V Vlachy
Journal:  J Phys Condens Matter       Date:  2018-11-12       Impact factor: 2.333

3.  Revisit PEG-Induced Precipitation Assay for Protein Solubility Assessment of Monoclonal Antibody Formulations.

Authors:  Martha J Scannell; Matthew W Hyatt; Ivan L Budyak; Mahlet A Woldeyes; Ying Wang
Journal:  Pharm Res       Date:  2021-10-13       Impact factor: 4.200

  3 in total

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