Rizzo V, Stankowski S, Schwarz G
Biochemistry. 1987 May 19;26(10):2751-9. doi: 10.1021/bi00384a015.
Interaction of the peptide antibiotic alamethicin with phospholipid vesicles has been monitored by changes in its circular dichroic and fluorescent properties. The data are consistent with an incorporation of the peptide in the lipid bilayer. Aggregation of alamethicin in the membrane phase is evident from a characteristic concentration dependence of the incorporation, reflecting the existence of a critical concentration. The data can be fully understood in terms of a theoretical approach that includes aggregation and thermodynamic nonideality. Thermodynamic parameters of the peptide-lipid interaction have been evaluated under a variety of conditions of temperature, ionic strength, and lipid type (saturated and unsaturated fatty acid chains). From the results obtained in this study, one can extrapolate to the incorporation behavior of alamethicin at low concentrations, as they are typical for measurements of conductance across planar lipid films. This leads to a simple explanation of the voltage-gating mechanism of alamethicin in a straightforward way.
已通过肽抗生素短杆菌肽与磷脂囊泡相互作用时其圆二色性和荧光特性的变化对该相互作用进行了监测。数据表明该肽掺入了脂质双层中。短杆菌肽在膜相中的聚集从掺入的特征浓度依赖性中明显可见,这反映了临界浓度的存在。这些数据可以通过一种包括聚集和热力学非理想性的理论方法得到充分理解。已在多种温度、离子强度和脂质类型(饱和和不饱和脂肪酸链)条件下评估了肽 - 脂质相互作用的热力学参数。从本研究获得的结果可以推断出低浓度下短杆菌肽的掺入行为,因为这些浓度是测量跨平面脂质膜电导时的典型浓度。这以一种直接的方式对短杆菌肽的电压门控机制给出了简单解释。