Toretsky Jeffrey A, Wright Peter E
Department of Oncology, Georgetown University, Washington, DC 20057
Department of Integrative Structural and Computational Biology and Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037 Department of Integrative Structural and Computational Biology and Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037.
J Cell Biol. 2014 Sep 1;206(5):579-88. doi: 10.1083/jcb.201404124.
The partitioning of intracellular space beyond membrane-bound organelles can be achieved with collections of proteins that are multivalent or contain low-complexity, intrinsically disordered regions. These proteins can undergo a physical phase change to form functional granules or other entities within the cytoplasm or nucleoplasm that collectively we term "assemblage." Intrinsically disordered proteins (IDPs) play an important role in forming a subset of cellular assemblages by promoting phase separation. Recent work points to an involvement of assemblages in disease states, indicating that intrinsic disorder and phase transitions should be considered in the development of therapeutics.
膜结合细胞器之外的细胞内空间划分可通过多价蛋白质集合或包含低复杂性、内在无序区域的蛋白质来实现。这些蛋白质可经历物理相变,在细胞质或核质中形成功能性颗粒或其他实体,我们将这些统称为“聚集体”。内在无序蛋白质(IDP)通过促进相分离在形成细胞聚集体的一个子集中发挥重要作用。最近的研究表明聚集体与疾病状态有关,这表明在治疗药物开发中应考虑内在无序和相变因素。