Jaffe Eileen K
BioMolecular Structure and Function Group, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Trends Biochem Sci. 2005 Sep;30(9):490-7. doi: 10.1016/j.tibs.2005.07.003.
Classic models for the allosteric regulation of protein function consider an equilibrium among protein structures of constant oligomeric multiplicity. The morpheein (mor-phee'-in) concept expands this model to include a dynamic equilibrium of protein structures wherein a protein monomer can exist in more than one conformation and each monomer conformation dictates a different quaternary structure of finite multiplicity and different functionality. The morpheein concept provides a new framework for understanding allosteric regulation, kinetic cooperativity and hysteresis. Porphobilinogen synthase constitutes a prototype morpheein ensemble comprising several interconverting quaternary structure isoforms; one monomer conformation dictates assembly of a high-activity octamer, whereas an alternative monomer conformation dictates assembly of a low-activity hexamer. It is proposed here that the behavior of some other allosteric enzymes reflect dynamic morpheein equilibrium systems and six candidate proteins are enumerated.
蛋白质功能变构调节的经典模型考虑的是具有恒定寡聚体多样性的蛋白质结构之间的平衡。形态素(morphee'-in)概念扩展了该模型,纳入了蛋白质结构的动态平衡,其中蛋白质单体可以以不止一种构象存在,并且每个单体构象决定了具有有限多样性和不同功能的不同四级结构。形态素概念为理解变构调节、动力学协同性和滞后现象提供了一个新框架。胆色素原合酶构成了一个形态素集合体原型,包含几种相互转化的四级结构异构体;一种单体构象决定了高活性八聚体的组装,而另一种单体构象决定了低活性六聚体的组装。本文提出,其他一些变构酶的行为反映了动态形态素平衡系统,并列举了六种候选蛋白质。