内在无序蛋白质
纳米技术
瓶颈
计算生物学
生化工程
计算机科学
化学
生物
生物物理学
材料科学
工程类
嵌入式系统
作者
Christian Parsbæk Pedersen,Pernille Seiffert,Inna Brakti,Katrine Bugge
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 195-209
被引量:12
标识
DOI:10.1007/978-1-0716-0524-0_9
摘要
Intrinsically disordered proteins (IDPs) have no single, fixed tertiary structure, yet they take on many vital functions in biology. In recent years, considerable effort has been put into the structural characterization of their conformational ensembles, to understand the link between the transient, short- and long-range organizations of IDPs and their functions. Such biophysical studies require substantial amounts of pure protein, representing a major bottleneck in the studies of IDPs. However, the unique physicochemical properties resulting from their compositional bias may be exploited for simple yet effective purification strategies. In this chapter, we provide tips and tricks for IDP production and describe the most important analyses to carry out before bringing an IDP of interest to the laboratory. We outline four purification protocols utilizing the unique properties of IDPs as well as some commonly encountered challenges and pitfalls.
科研通智能强力驱动
Strongly Powered by AbleSci AI