UT/ORNL Center for Molecular Biophysics, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
Biophys Chem. 2012 Jan;160(1):20-7. doi: 10.1016/j.bpc.2011.08.007. Epub 2011 Sep 10.
The effect of the charged lidocaine on the structure and dynamics of DMPC/DMPG (mass fraction of 95/5) unilamellar vesicles has been investigated. Changes in membrane organization caused by the presence of lidocaine were detected through small angle neutron scattering experiments. Our results suggest that the presence of lidocaine in the vicinity of the headgroups of lipid membranes leads to an increase of the area per lipid molecule and to a decrease of membrane thickness. Such changes in membrane structure may induce disordering of the tail group. This scenario explains the reduction of the main transition temperature of lipid membranes, as the fraction of lidocaine per lipid molecules increases, which was evident from differential scanning calorimetry results. Furthermore neutron spin echo spectroscopy was used for the dynamics measurements and the results reveal that presence of charged lidocaine increases the bending elasticity of the lipid membranes in the fluid phase and slows the temperature-dependent change of bending elasticity across the main transition temperature.
已研究带电荷的利多卡因对 DMPC/DMPG(质量分数为 95/5)单层囊泡结构和动力学的影响。通过小角中子散射实验检测到利多卡因存在引起的膜组织变化。我们的结果表明,利多卡因存在于脂质膜头部基团附近会导致每个脂质分子的面积增加,并且膜厚度减小。这种膜结构的变化可能会导致尾部基团的无序化。这种情况解释了脂质膜的主要相变温度降低,随着脂质分子中利多卡因的比例增加,这从差示扫描量热法结果中显而易见。此外,中子自旋回波光谱用于动力学测量,结果表明带电荷的利多卡因增加了流体相中的脂质膜弯曲弹性,并减缓了主相变温度下弯曲弹性随温度的变化。