An Integrated Experimental and Modeling Approach for Crystallization of Complex Biotherapeutics

IF 3.4 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Vivekananda Bal, Moo Sun Hong, Jacqueline M. Wolfrum, Paul W. Barone, Stacy L. Springs, Anthony J. Sinskey, Robert M. Kotin and Richard D. Braatz*, 
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Abstract

Crystallization of proteins, specifically proteins of medical relevance, is performed for various reasons, such as to understand the protein structure and to design therapies. Obtaining kinetic constants in rate laws for nucleation and growth of advanced biotherapeutics such as capsids, an assembly of macromolecules, is challenging and essential to the design of crystallization processes. In this work, coupled population balance and species balance equations are developed to extract nucleation and growth kinetics for the crystallization of recombinant adeno-associated virus (rAAV) capsids. A comparison of model results with that of experimental data for capsid crystallization in a hanging-drop vapor diffusion system shows that the slow rate of vapor diffusion from the droplet controls the initial nucleation and growth processes, and the capsid nucleation occurs via heterogeneous nucleation in the microdroplet. Results also show that the capsids, which are of very high molecular weight (∼3.6 MDa), have a similar tendency to nucleate as small organic molecules such as glycine (∼75 Da), low-molecular-weight proteins, and small-molecule active pharmaceutical ingredients due to their ball-shaped outer structure/shape. Capsids also show a prolonged nucleation period as for proteins and other macromolecules but have a slow growth rate with a growth rate prefactor seven orders of magnitude smaller than that of lysozyme. The capsid crystal growth rate is weakly sensitive to supersaturation compared to lysozyme and is limited by the transport of capsids due to slow Brownian motion resulting from the very high molecular weight.

We developed a mathematical model based on population balance equation and compared the simulation results with the in-house experimental measurements for temporal evolution of crystal growth rate, crystal size distribution, total number density, total length, total radius, total surface area, and total volume.

复杂生物治疗药物结晶的综合实验与建模方法
蛋白质的结晶,特别是与医学相关的蛋白质,是出于各种原因进行的,例如了解蛋白质结构和设计治疗方法。获得先进生物治疗药物(如衣壳)成核和生长的速率定律中的动力学常数,对于设计结晶过程是具有挑战性的,也是必不可少的。在这项工作中,建立了耦合的种群平衡和物种平衡方程,以提取重组腺相关病毒(rAAV)衣壳结晶的成核和生长动力学。悬垂液滴蒸汽扩散系统中衣壳结晶的模型结果与实验数据的对比表明,微液滴缓慢的蒸汽扩散速率控制了衣壳的初始成核和生长过程,衣壳的成核是通过微液滴的非均相成核进行的。结果还表明,由于其球形的外部结构/形状,具有非常高分子量(~ 3.6 MDa)的衣壳具有与甘氨酸(~ 75 Da)、低分子量蛋白质和小分子活性药物成分等小有机分子相似的成核倾向。衣壳与蛋白质和其他大分子一样具有较长的成核期,但其生长速度较慢,其生长速度因子比溶菌酶小7个数量级。与溶菌酶相比,衣壳晶体的生长速率对过饱和度的敏感性较弱,并且由于极高的分子量导致衣壳的缓慢布朗运动而受到衣壳运输的限制。我们建立了基于种群平衡方程的数学模型,并将模拟结果与室内实验测量结果进行了比较,分析了晶体生长速率、晶体尺寸分布、总数密度、总长度、总半径、总表面积和总体积的时间演变。
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来源期刊
Crystal Growth & Design
Crystal Growth & Design 化学-材料科学:综合
CiteScore
6.30
自引率
10.50%
发文量
650
审稿时长
1.9 months
期刊介绍: The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials. Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.
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