School of Science, STEM College, RMIT University, 124 La Trobe Street, Melbourne, VIC 3000, Australia.
School of Science, STEM College, RMIT University, 124 La Trobe Street, Melbourne, VIC 3000, Australia.
J Colloid Interface Sci. 2022 Feb 15;608(Pt 2):1173-1190. doi: 10.1016/j.jcis.2021.10.087. Epub 2021 Oct 19.
Ionic liquids (ILs) have been used in solvents for proteins in many applications, including biotechnology, pharmaceutics, and medicine due to their tunable physicochemical and biological properties. Protein aggregation is often undesirable, and predominantly occurs during bioprocesses, while the aggregation process can be reversible or irreversible and the aggregates formed can be native/non-native and soluble/insoluble. Recent studies have clearly identified key properties of ILs and IL-water mixtures related to protein performance, suggesting the use of the tailorable properties of ILs to inhibit protein aggregation, to promote protein crystallization, and to control protein aggregation pathways. This review discusses the critical properties of IL and IL-water mixtures and presents the latest understanding of the protein aggregation pathways and the development of IL systems that affect or control the protein aggregation process. Through this feature article, we hope to inspire further advances in understanding and new approaches to controlling protein behavior to optimize bioprocesses.
离子液体 (ILs) 由于其可调节的物理化学和生物特性,已在许多应用中被用作蛋白质的溶剂,包括生物技术、制药和医学。蛋白质聚集通常是不理想的,主要发生在生物过程中,而聚集过程可以是可逆的或不可逆的,形成的聚集体可以是天然/非天然的和可溶/不可溶的。最近的研究清楚地确定了与蛋白质性能相关的离子液体和离子液体-水混合物的关键性质,表明可以利用离子液体的可调节性质来抑制蛋白质聚集、促进蛋白质结晶和控制蛋白质聚集途径。本文讨论了离子液体和离子液体-水混合物的关键性质,并介绍了最新的蛋白质聚集途径的理解以及影响或控制蛋白质聚集过程的离子液体系统的发展。通过这篇专题文章,我们希望激发人们进一步深入了解和探索控制蛋白质行为的新方法,以优化生物过程。