Department of Dosage Form Design and Development, Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, 20878, USA.
Dynamics of Macromolecular Assembly Section, Laboratory of Cellular Imaging and Macromolecular Biophysics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, 20817, USA.
Sci Rep. 2021 Mar 11;11(1):5741. doi: 10.1038/s41598-021-84946-8.
Weak macromolecular interactions assume a dominant role in the behavior of highly concentrated solutions, and are at the center of a variety of fields ranging from colloidal chemistry to cell biology, neurodegenerative diseases, and manufacturing of protein drugs. They are frequently measured in different biophysical techniques in the form of second virial coefficients, and nonideality coefficients of sedimentation and diffusion, which may be related mechanistically to macromolecular distance distributions in solution and interparticle potentials. A problem arises for proteins where reversible self-association often complicates the concentration-dependent behavior, such that grossly inconsistent coefficients are measured in experiments based on different techniques, confounding quantitative conclusions. Here we present a global multi-method analysis that synergistically bridges gaps in resolution and sensitivity of orthogonal techniques. We demonstrate the method with a panel of monoclonal antibodies exhibiting different degrees of self-association. We show how their concentration-dependent behavior, examined by static and dynamic light scattering and sedimentation velocity, can be jointly described in a self-consistent framework that separates nonideality coefficients from self-association properties, and thereby extends the quantitative interpretation of nonideality coefficients to probe dynamics in highly concentrated protein solutions.
弱的高分子相互作用在高浓度溶液的行为中起着主导作用,它们处于从胶体化学到细胞生物学、神经退行性疾病和蛋白质药物制造等多种领域的中心。它们经常以第二维里系数和沉降与扩散的非理想系数的形式,通过不同的生物物理技术进行测量,这些系数在机制上可能与溶液中高分子的距离分布和颗粒间的势能有关。对于蛋白质来说,存在一个问题,即可逆的自组装常常使浓度依赖性行为变得复杂,以至于基于不同技术的实验测量到的粗粒度不一致的系数,使得定量结论变得混乱。在这里,我们提出了一种全局多方法分析,该分析协同弥合了正交技术在分辨率和灵敏度上的差距。我们用一组表现出不同自组装程度的单克隆抗体来演示该方法。我们展示了如何通过静态和动态光散射以及沉降速度来检查它们的浓度依赖性行为,如何在一个自洽的框架中联合描述这些行为,该框架将非理想系数与自组装特性分离,从而将非理想系数的定量解释扩展到探测高浓度蛋白质溶液中的动力学。