溶解度
合理设计
蛋白质聚集
计算机科学
蛋白质设计
化学
材料科学
纳米技术
蛋白质结构
生物化学
有机化学
作者
Aleksander Kuriata,Aleksandra E. Badaczewska-Dawid,Jordi Pujols,Salvador Ventura,Sebastian Kmiecik
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 17-40
被引量:1
标识
DOI:10.1007/978-1-0716-1546-1_2
摘要
Protein aggregation is a major hurdle in the development and manufacturing of protein-based therapeutics. Development of aggregation-resistant and stable protein variants can be guided by rational redesign using computational tools. Here, we describe the architecture and functionalities of the Aggrescan3D (A3D) standalone package for the rational design of protein solubility and aggregation properties based on three-dimensional protein structures. We present the case studies of the three therapeutic proteins, including antibodies, exploring the practical use of the A3D standalone tool. The case studies demonstrate that protein solubility can be easily improved by the A3D prediction of non-destabilizing amino acid mutations at the protein surfaces.
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