Protein structural conformation and not second virial coefficient relates to long-term irreversible aggregation of a monoclonal antibody and ovalbumin in solution

被引:47
作者
Bajaj, Harminder
Sharma, Vikas K.
Badkar, Advait
Zeng, David
Nema, Sandeep
Kalonia, Devendra S. [1 ]
机构
[1] Univ Connecticut, Dept Pharmaceut Sci, Storrs, CT 06269 USA
[2] Pfizer Biol, St Louis, MO 63017 USA
[3] Univ Connecticut, Sch Pharm, U 3092, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
antibody formulation; monoclonal antibody; protein aggregation; protein stability; second viral coefficient;
D O I
10.1007/s11095-006-0018-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The purpose of the study was to investigate the relationship of the second virial coefficient, B-22, to the extent of irreversible protein aggregation upon storage. Methods. A monoclonal antibody and ovalbumin were incubated at 37 degrees C (3 months) under various solution conditions to monitor the extent of aggregation. The B-22 values of these proteins were determined under similar solution conditions by a modified method of flow-mode static light scattering. The conformation of these proteins was studied using circular dichroism (CD) spectroscopy and second-derivative Fourier transform infrared spectroscopy. Results. Both proteins readily aggregated at pH 4.0 (no aggregation observed at pH 7.4); the extent of aggregation varied with the ionic strength and the presence of cosolutes (sucrose, glycine, and Tween 80). Debye plots of the monoclonal antibody showed moderate attractive interactions at pH 7.4, whereas, at pH 4.0, nonlinear plots were obtained, indicating self-association. CD studies showed partially unfolded structure of antibody at pH 4.0 compared with that at pH 7.4. In the case of ovalbumin, similar B-22 values were obtained in all solution conditions irrespective of whether the protein aggregated or not. CD studies of ovalbumin indicated the presence of a fraction of completely unfolded as well as partially unfolded species at pH 4.0 compared with that at pH 7.4. Conclusions. The formation of a structurally altered state is a must for irreversible aggregation to proceed. Because this aggregation-prone species could be an unfolded species present in a small fraction compared with that of the native state or it could be a partially unfolded state whose net interactions are not significantly different compared with those of the native state, yet the structural changes are sufficient to lead to long-term aggregation, it is unlikely that B-22 will correlate with long-term aggregation.
引用
收藏
页码:1382 / 1394
页数:13
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