Shiraki Kentaro, Mimura Masahiro, Nishinami Suguru, Ura Tomoto
Faculty of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8573, Japan.
Biophys Rev. 2020 Apr;12(2):587-592. doi: 10.1007/s12551-020-00682-9. Epub 2020 Mar 12.
This review briefly summarizes the effect of additives on the formation of liquid droplets and aggregates of proteins. Proteins have the property of forming liquid droplets and aggregates both in vivo and in vitro. The liquid droplets of proteins are mainly stabilized by electrostatic and cation-π interactions, whereas the amorphous aggregates are mainly stabilized by hydrophobic interactions. Crowders usually stabilize liquid droplets, whereas ions and hexandiols destabilize the droplets. Additives such as kosmotropes, sugars, osmolytes, and crowders promote the formation of amorphous aggregates, whereas additives such as arginine and chaotropes can prevent the formation of amorphous aggregates. Further, amyloid has a different mechanism for its formation from amorphous aggregates because it is primarily stabilized by a cross-β structure. These systematic analyses of additives will provide clues to controlling protein aggregations and will aid the true understanding of the transition of proteins from liquid droplets and aggregates.
本综述简要总结了添加剂对蛋白质液滴和聚集体形成的影响。蛋白质在体内和体外均具有形成液滴和聚集体的特性。蛋白质液滴主要通过静电和阳离子-π相互作用得以稳定,而非晶态聚集体主要通过疏水相互作用得以稳定。拥挤剂通常会稳定液滴,而离子和己二醇会使液滴不稳定。促溶剂、糖类、渗透剂和拥挤剂等添加剂会促进非晶态聚集体的形成,而精氨酸和离液剂等添加剂可防止非晶态聚集体的形成。此外,淀粉样蛋白的形成机制与非晶态聚集体不同,因为它主要通过交叉β结构得以稳定。对添加剂的这些系统分析将为控制蛋白质聚集提供线索,并有助于真正理解蛋白质从液滴和聚集体的转变。