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Phase transitions in human IgG solutions

机译:人IgG溶液中的相变

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Protein condensations, such as crystallization, liquid-liquid phase separation, aggregation, and gelation, have been observed in concentrated antibody solutions under various solution conditions. While most IgG antibodies are quite soluble, a few outliers can undergo condensation under physiological conditions. Condensation of IgGs can cause serious consequences in some human diseases and in biopharmaceutical formulations. The phase transitions underlying protein condensations in concentrated IgG solutions is also of fundamental interest for the understanding of the phase behavior of non-spherical protein molecules. Due to the high solubility of generic IgGs, the phase behavior of IgG solutions has not yet been well studied. In this work, we present an experimental approach to study IgG solutions in which the phase transitions are hidden below the freezing point of the solution. Using this method, we have investigated liquid-liquid phase separation of six human myeloma IgGs and two recombinant pharmaceutical human IgGs. We have also studied the relation between crystallization and liquid-liquid phase separation of two human cryoglobulin IgGs. Our experimental results reveal several important features of the generic phase behavior of IgG solutions: (1) the shape of the coexistence curve is similar for all IgGs but quite different from that of quasi-spherical proteins; (2) all IgGs have critical points located at roughly the same protein concentration at ~100 mg/ml while their critical temperatures vary significantly; and (3) the liquid-liquid phase separation in IgG solutions is metastable with respect to crystallization. These features of phase behavior of IgG solutions reflect the fact that all IgGs have nearly identical molecular geometry but quite diverse net inter-protein interaction energies. This work provides a foundation for further experimental and theoretical studies of the phase behavior of generic IgGs as well as outliers with large propensity to condense. The investigation of the phase diagram of IgG solutions is of great importance for the understanding of immunoglobulin deposition diseases as well as for the understanding of the colloidal stability of IgG pharmaceutical formulations.
机译:在各种溶液条件下,在浓缩抗体溶液中都观察到蛋白质缩合,例如结晶,液-液相分离,聚集和胶凝。尽管大多数IgG抗体都非常易溶,但少数异常值会在生理条件下发生缩合。 IgG的缩合会在某些人类疾病和生物药物制剂中造成严重后果。浓缩IgG溶液中蛋白质缩合的基础相变对于理解非球形蛋白质分子的相行为也具有根本的意义。由于通用IgG的高溶解度,IgG溶液的相行为尚未得到很好的研究。在这项工作中,我们提出了一种实验方法来研究IgG溶液,其中相变隐藏在溶液的冰点以下。使用这种方法,我们研究了六个人类骨髓瘤IgG和两个重组药物人类IgG的液-液相分离。我们还研究了两种人冷球蛋白IgG的结晶与液相分离的关系。我们的实验结果揭示了IgG溶液的通用相行为的几个重要特征:(1)所有IgG的共存曲线形状相似,但与准球形蛋白质的相差很大; (2)所有IgG的临界点都在〜100 mg / ml的大致相同的蛋白质浓度处,而它们的临界温度却相差很大; (3)IgG溶液中的液-液相分离相对于结晶是亚稳态的。 IgG溶液的相行为的这些特征反映了以下事实:所有IgG都具有几乎相同的分子几何结构,但蛋白质间相互作用的净能量却非常不同。这项工作为进一步的实验和理论研究奠定基础,以研究通用IgG的相态行为以及具有较大凝结倾向的离群值。 IgG溶液相图的研究对于理解免疫球蛋白沉积疾病以及对IgG药物制剂的胶体稳定性至关重要。

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