Protein Modality and Bulk Concentration Impact the Evolution of Rheological Properties of IgG mAb and Fc-Fusion Protein Films at an Air-Water Interface.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Valerie P Griffin, Estephanie L Nottar Escobar, Ankit Kanthe, Madhushree Gokhale, Prajnaparamita Dhar
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Abstract

Therapeutic proteins, such as monoclonal antibodies (mAbs), can form two-dimensional films at the air-water interface, which, when ruptured or stressed, can lead to protein instability in solution. However, the details of the dynamics of mAb film formation, particularly the transitions in the rheological properties of the film, are not well understood. The emergence of novel protein-based modalities also raises the question of whether our understanding of mAb film formation can be extended to other novel biotherapeutic modalities. This work aims to understand the dynamics of film formation in novel therapeutic proteins by correlating protein adsorption kinetics, measured using surface tensiometry, with the evolution of the interfacial rheological properties, measured using a passive microrheology technique, for two protein modalities: IgG mAb and Fc-Fusion protein. Further, to accurately record how differences in packing density at the interface might lead to differences in the rheological properties in these different protein modalities during film aging, the bulk protein concentration was varied over 3 orders of magnitude. Our results indicate that the multistage protein adsorption process seen in both protein modalities can result in transitions in film rheology from purely viscous to viscoelastic and elastic films with time, depending on the bulk concentration and protein modality. Fc-Fusion proteins demonstrated an earlier onset of viscoelastic film transition compared with IgG mAbs for all bulk concentrations studied. Further, polysorbate 80 (PS80), often added to protein solutions to mitigate protein aggregation, prevents this transition in IgG mAb solutions but not in Fc-Fusion protein solutions. Together, our results provide rheological characterization of the protein films during adsorption and film aging in these novel biotherapeutics and will help inform the development of appropriate mitigation strategies to maintain their interfacial stability.

蛋白质形态和体积浓度影响IgG单抗和fc融合蛋白膜在空气-水界面的流变特性演变
治疗性蛋白质,如单克隆抗体(mab),可以在空气-水界面形成二维膜,当破裂或受压时,可导致溶液中的蛋白质不稳定。然而,单克隆抗体薄膜形成的动力学细节,特别是薄膜流变特性的转变,还没有得到很好的理解。新的基于蛋白质的模式的出现也提出了一个问题,即我们对mAb膜形成的理解是否可以扩展到其他新的生物治疗模式。这项工作旨在通过将蛋白质吸附动力学(使用表面张力测定法测量)与界面流变特性的演变(使用被动微流变学技术测量)相关联,了解新型治疗蛋白中膜形成的动力学。两种蛋白质模式:IgG单抗和fc融合蛋白。此外,为了准确记录在膜老化过程中,界面处堆积密度的差异如何导致这些不同蛋白质形态的流变特性差异,体积蛋白质浓度变化超过3个数量级。我们的研究结果表明,根据体积浓度和蛋白质形态的不同,两种蛋白质形态下的多级蛋白质吸附过程可以导致膜流变从纯粘性到粘弹性和弹性膜随时间的转变。与IgG单克隆抗体相比,fc融合蛋白在所有体积浓度下都表现出更早的粘弹性膜转变。此外,聚山梨酸酯80 (PS80)通常添加到蛋白质溶液中以减轻蛋白质聚集,在IgG单抗溶液中阻止这种转变,但在Fc-Fusion蛋白溶液中没有。总之,我们的研究结果提供了这些新型生物疗法中蛋白质膜在吸附和膜老化过程中的流变特性,并将有助于制定适当的减缓策略以保持其界面稳定性。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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