Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
J Mol Biol. 2018 Nov 2;430(23):4806-4820. doi: 10.1016/j.jmb.2018.06.038. Epub 2018 Jun 23.
The formation of membrane-less organelles and compartments by protein phase separation is an important way in which cells organize their cytoplasm and nucleoplasm. In vitro phase separation assays with purified proteins have become the standard way to investigate proteins that form membrane-less compartments. By now, various proteins have been purified and tested for their ability to phase separate and form liquid condensates in vitro. However, phase-separating proteins are often aggregation-prone and difficult to purify and handle. As a consequence, the results from phase separation assays often differ between labs and are not easily reproduced. Thus, there is an urgent need for high-quality proteins, standardized procedures, and generally agreed-upon practices for protein purification and conducting phase separation assays. This paper provides protocols for protein purification and guides the user through the practicalities of in vitro protein phase separation assays, including best-practice approaches and pitfalls to avoid. We believe that this compendium of protocols and practices will provide a useful resource for scientists studying the phase behavior of proteins.
无膜细胞器和隔室的形成通过蛋白质相分离是细胞组织细胞质和核质的一种重要方式。用纯化蛋白进行的体外相分离测定已成为研究形成无膜隔室的蛋白质的标准方法。到目前为止,已经纯化了各种蛋白质,并测试了它们在体外相分离和形成液滴的能力。然而,相分离蛋白往往容易聚集,且难以纯化和处理。因此,相分离测定的结果在不同的实验室之间往往存在差异,并且不容易重现。因此,迫切需要高质量的蛋白质、标准化的程序以及用于蛋白质纯化和进行相分离测定的普遍接受的实践。本文提供了蛋白质纯化的方案,并指导用户进行体外蛋白质相分离测定的实际操作,包括最佳实践方法和避免的陷阱。我们相信,本协议和实践的汇编将为研究蛋白质相行为的科学家提供有用的资源。