Materials Processing Center, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
J Chem Phys. 2013 Sep 28;139(12):121904. doi: 10.1063/1.4811345.
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.
蛋白质凝聚物,如结晶、液-液相分离、聚集和胶凝,在各种溶液条件下都在浓缩的抗体溶液中被观察到。虽然大多数 IgG 抗体非常可溶性,但少数异常抗体在生理条件下可以发生凝聚。IgG 的凝聚会在一些人类疾病和生物制药制剂中造成严重后果。浓缩 IgG 溶液中蛋白质凝聚的相变对于理解非球形蛋白质分子的相行为也具有根本意义。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,我们研究了六种人类骨髓瘤 IgG 和两种重组药物人 IgG 的液-液相分离。我们还研究了两种人类冷球蛋白 IgG 的结晶与液-液相分离之间的关系。我们的实验结果揭示了 IgG 溶液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形状大不相同;(2)所有 IgG 的临界点都位于大约 100mg/ml 的相似蛋白浓度,而它们的临界温度差异很大;(3)IgG 溶液中的液-液相分离相对于结晶是亚稳的。这些 IgG 溶液相行为的特征反映了这样一个事实,即所有 IgG 具有几乎相同的分子几何形状,但净蛋白质间相互作用能差异很大。这项工作为进一步实验和理论研究通用 IgG 以及具有较大凝聚倾向的异常 IgG 的相行为提供了基础。研究 IgG 溶液的相图对于理解免疫球蛋白沉积疾病以及理解 IgG 药物制剂的胶体稳定性都具有重要意义。