Roux M, Bloom M
Department of Physics, University of British Columbia, Vancouver, Canada.
Biochemistry. 1990 Jul 31;29(30):7077-89. doi: 10.1021/bi00482a019.
The binding of calcium, magnesium, lithium, potassium, and sodium to membrane bilayers of 5 to 1 (M/M) 1-palmitoyl-2-oleoylphosphatidylcholine (POPC) and 1-palmitoyl- 2-oleoylphosphatidylserine (POPS) was investigated by using deuterium nuclear magnetic resonance (2H NMR). Both lipids were deuteriated on their polar headgroups, and spectra were obtained at 25 degrees C in the liquid-crystalline phase as a function of salt concentration. The spectra obtained with calcium were correlated with 45CaCl2 binding studies to determine the effective membrane-bound calcium at low calcium binding, up to 0.78 calcium per POPS. Deuterium quadrupolar splittings of both POPC and POPS headgroups were shown to be very sensitive to calcium binding. The behavior of these two headgroups over a wide range of CaCl2 concentrations suggests that Ca2+ binding occurs in at least two steps, the first step being achieved with 0.5 M CaCl2, with a stoichiometry of 0.5 Ca2+ per POPS. Correlations of the deuterium Ca2+ binding data with related data obtained after incorporation of a cationic integral peptide showed that the effects of these two cationic molecules of the POPS headgroup are qualitatively similar, and provided further support for two-step Ca2+ binding to the POPC/POPS 5:1 membranes. The corresponding data obtained with magnesium, lithium, and potassium indicate that these cations interact with both the choline and serine headgroups. The amplitudes of headgroup perturbations could be partly correlated to the relative affinities of the metallic cations for the lipid membrane. The two-step binding described with Ca2+ appears to be relevant to the Mg2+ data, and in certain limits to the Li+ data. The data were interpreted in terms of conformational changes of the lipid headgroups induced by an electric field due to the charges of the membrane-bound metallic cations. A conformational change of the serine headgroup induced by the membrane-bound charges is proposed. We propose that the metallic cations can be differentiated on the basis of their respective spatial distribution functions relative to the choline and serine headgroups. According to this interpretation, the divalent cations Ca2+ and Mg2+ are more deeply buried in the membrane than monovalent Na+ and K+, the case of Li+ being intermediate of the latter two. This conclusion is discussed in relation to fundamental theories of the spatial distribution of ions near the interface between water and smooth charged solid surfaces.
通过使用氘核磁共振(2H NMR)研究了钙、镁、锂、钾和钠与5比1(摩尔/摩尔)的1-棕榈酰-2-油酰磷脂酰胆碱(POPC)和1-棕榈酰-2-油酰磷脂酰丝氨酸(POPS)膜双层的结合。两种脂质的极性头部都进行了氘代,并在25摄氏度的液晶相中作为盐浓度的函数获得了光谱。用钙获得的光谱与45CaCl2结合研究相关,以确定低钙结合时的有效膜结合钙,最高可达每个POPS 0.78个钙。POPC和POPS头部基团的氘四极分裂显示对钙结合非常敏感。这两个头部基团在广泛的CaCl2浓度范围内的行为表明,Ca2+结合至少分两步进行,第一步在0.5 M CaCl2时实现,化学计量比为每个POPS 0.5个Ca2+。氘Ca2+结合数据与掺入阳离子整合肽后获得的相关数据的相关性表明,POPS头部基团的这两种阳离子分子的作用在质量上是相似的,并为Ca2+与POPC/POPS 5:1膜的两步结合提供了进一步的支持。用镁、锂和钾获得的相应数据表明,这些阳离子与胆碱和丝氨酸头部基团都相互作用。头部基团扰动的幅度可以部分地与金属阳离子对脂质膜的相对亲和力相关。用Ca2+描述的两步结合似乎与Mg2+数据相关,在一定程度上也与Li+数据相关。这些数据根据膜结合金属阳离子的电荷引起的电场诱导的脂质头部基团的构象变化进行了解释。提出了由膜结合电荷诱导的丝氨酸头部基团的构象变化。我们提出,可以根据金属阳离子相对于胆碱和丝氨酸头部基团的各自空间分布函数来区分它们。根据这种解释,二价阳离子Ca2+和Mg2+比单价Na+和K+更深入地埋在膜中,Li+的情况介于后两者之间。结合水与光滑带电固体表面界面附近离子空间分布的基本理论对这一结论进行了讨论。