Kimelberg H K
Mol Cell Biochem. 1976 Feb 25;10(3):171-90. doi: 10.1007/BF01731688.
Recent studies on the interactions of soluble proteins, membrane proteins and enzymes with phospholipid model membranes are reviewed. Similarities between the properties of such systems and the behavior of biomembranes, such as alterations in the redox potential of cytochrome c after binding to membranes and effects of phospholipid fluidity on (Na+K) ATPase activity, are emphasized. The degree of correspondence between the behavior of model systems and natural membranes encourages the continuing use of model membranes in studies on protein-lipid interactions. However, some of the data on the increase of surface pressure of phospholipid monolayers by proteins and increases in the permeability of liposomes indicate that many soluble proteins also have a capability to interact hydrophobically with phospholipids. Thus a sharp distinction between both peripheral and integral membrane proteins and non-membrane proteins are not seen by these techniques. Cautious use of such studies, however, should lead to greater understanding of the molecular basis of cell membrane structure and function in normal and pathological states. Studies implicating protein-lipid interactions and (Na+K) ATPase activity in membrane alterations in disease states are also briefly discussed.
本文综述了近期关于可溶性蛋白质、膜蛋白和酶与磷脂模型膜相互作用的研究。强调了此类系统的性质与生物膜行为之间的相似性,例如细胞色素c与膜结合后氧化还原电位的变化以及磷脂流动性对(Na + K)ATP酶活性的影响。模型系统与天然膜行为之间的对应程度鼓励在蛋白质 - 脂质相互作用研究中继续使用模型膜。然而,一些关于蛋白质使磷脂单层表面压力增加以及脂质体通透性增加的数据表明,许多可溶性蛋白质也具有与磷脂疏水相互作用的能力。因此,通过这些技术无法明确区分外周膜蛋白、整合膜蛋白和非膜蛋白。然而,谨慎使用此类研究应有助于更深入地理解正常和病理状态下细胞膜结构和功能的分子基础。本文还简要讨论了疾病状态下涉及蛋白质 - 脂质相互作用和(Na + K)ATP酶活性与膜改变的研究。