Dzikovski Boris G, Borbat Petr P, Freed Jack H
Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14583-1301, USA.
Biophys J. 2004 Nov;87(5):3504-17. doi: 10.1529/biophysj.104.044305. Epub 2004 Aug 23.
Gramicidin A was studied by continuous wave electron spin resonance (CW-ESR) and by double-quantum coherence electron spin resonance (DQC-ESR) in several lipid membranes (using samples that were macroscopically aligned by isopotential spin-dry ultracentrifugation) and vesicles. As a reporter group, the nitroxide spin-label was attached at the C-terminus yielding the spin-labeled product (GAsl). ESR spectra of aligned membranes containing GAsl show strong orientation dependence. In DPPC and DSPC membranes at room temperature the spectral shape is consistent with high ordering, which, in conjunction with the observed high polarity of the environment of the nitroxide, is interpreted in terms of the nitroxide moiety being close to the membrane surface. In contrast, spectra of GAsl in DMPC membranes indicate deeper embedding and tilt of the NO group. The GAsl spectrum in the DPPC membrane at 35 degrees C (the gel to Pbeta phase transition) exhibits sharp changes, and above this temperature becomes similar to that of DMPC. The dipolar spectrum from DQC-ESR clearly indicates the presence of pairs in DMPC membranes. This is not the case for DPPC, rapidly frozen from the gel phase; however, there are hints of aggregation. The interspin distance in the pairs is 30.9 A, in good agreement with estimates for the head-to-head GAsl dimer (the channel-forming conformation), which matches the hydrophobic thickness of the DMPC bilayer. Both DPPC and DSPC, apparently as a result of hydrophobic mismatch between the dimer length and bilayer thickness, do not favor the channel formation in the gel phase. In the Pbeta and Lalpha phases of DPPC (above 35 degrees C) the channel dimer forms, as evidenced by the DQC-ESR dipolar spectrum after rapid freezing. It is associated with a lateral expansion of lipid molecules and a concomitant decrease in bilayer thickness, which reduces the hydrophobic mismatch. A comparison with studies of dimer formation by other physical techniques indicates the desirability of using low concentrations of GA (approximately 0.4-1 mol %) accessible to the ESR methods employed in the study, since this yields non-interacting dimer channels.
采用连续波电子自旋共振(CW-ESR)和双量子相干电子自旋共振(DQC-ESR)技术,在几种脂质膜(使用通过等势自旋干燥超速离心宏观排列的样品)和囊泡中对短杆菌肽A进行了研究。作为报告基团,氮氧自旋标记连接在C端,得到自旋标记产物(GAsl)。含有GAsl的排列膜的ESR光谱显示出强烈的取向依赖性。在室温下的DPPC和DSPC膜中,光谱形状与高度有序一致,这与观察到的氮氧环境的高极性相结合,被解释为氮氧部分靠近膜表面。相比之下,GAsl在DMPC膜中的光谱表明NO基团更深地嵌入和倾斜。DPPC膜在35℃(凝胶到Pβ相转变)时的GAsl光谱表现出急剧变化,高于此温度后变得与DMPC的光谱相似。DQC-ESR的偶极光谱清楚地表明DMPC膜中存在成对现象。从凝胶相快速冷冻的DPPC则不是这种情况;然而,有聚集的迹象。成对中的自旋间距离为30.9 Å,与头对头GAsl二聚体(通道形成构象)的估计值非常吻合,该二聚体与DMPC双层的疏水厚度相匹配。显然,由于二聚体长度与双层厚度之间的疏水不匹配,DPPC和DSPC在凝胶相中都不利于通道形成。在DPPC的Pβ和Lα相(高于35℃)中,快速冷冻后的DQC-ESR偶极光谱证明形成了通道二聚体。它与脂质分子的横向扩展以及双层厚度的相应减小有关,这减少了疏水不匹配。与其他物理技术对二聚体形成的研究进行比较表明,使用该研究中ESR方法可检测的低浓度GA(约0.4-1 mol%)是可取的,因为这会产生非相互作用的二聚体通道。