Urbina J A, Pekerar S, Le H B, Patterson J, Montez B, Oldfield E
Department of Chemistry, University of Illinois at Urbana-Champaign 61801, USA.
Biochim Biophys Acta. 1995 Sep 13;1238(2):163-76. doi: 10.1016/0005-2736(95)00117-l.
We report the results of a comparative study of the molecular order and dynamics of phosphatidylcholine (PC) bilayer membranes in the absence and presence of cholesterol, ergosterol and lanosterol, using deuterium (2H) nuclear magnetic resonance (NMR) of deuterated phospholipid molecules, in addition to solid state 13C and 31P-NMR. Using dimyristoylphosphatidylcholines (DMPCs) specifically labeled at positions 2', 3', 4', 6', 8', 10' and 12' of the sn-2 chain together with the perdeuterated 2-[2H27]DMPC derivative, the order profile for 9 of the 13 methylene groups of the sn-2 chain was established at 25 degrees C for DMPC, DMPC/cholesterol, DMPC/ergosterol and DMPC/lanosterol membranes, at a fixed sterol/phospholipid mol ratio of 30%, and in the presence of excess water. The overall ordering effects were found to be ergosterol > cholesterol >> lanosterol. Transverse relaxation (T2e) studies of these systems indicated that while for DMPC, DMPC/cholesterol and DMPC/ergosterol the relative relaxation rates were in qualitative agreement with models which assume cooperative motions of the bilayer molecules as the main relaxation mechanism, those in DMPC/lanosterol were anomalously high, suggesting alterations of lipid packing. Using dipalmitoylphosphatidylcholine (DPPC) deuterated at the trimethylammonium group of the choline moiety, we found that the differential ordering and motional effects induced by the sterols in the acyl chains were also reflected in the headgroup, both in the gel (L beta) and liquid-crystalline phases. 13C and 1H spin dynamics studies of these systems, including cross-polarization, rotating frame longitudinal relaxation and dipolar echo relaxation rates showed that the mobility of the different regions of the phospholipid molecules in the binary lipid systems were inversely correlated with the ordering effects induced by the sterols. A novel combination of C-D bond order parameters (obtained by 2H-NMR) and 13C-1H cross polarization rates confirmed these results. The effects of the same sterols at the same molar proportion on the unsaturated lipid 1-[2H31]palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (2H31-POPC) at 25 and 35 degrees C were different from those observed on DMPC and showed ordering effects which are largest for cholesterol, while ergosterol and lanosterol produced significantly smaller effects. Transverse relaxation studies indicate that while cholesterol does not perturb cooperative motions in POPC, both ergosterol and lanosterol do. Again, high-resolution solid state 13C-NMR studies support the conclusions of the 2H-NMR experiments.(ABSTRACT TRUNCATED AT 400 WORDS)
我们报告了一项比较研究的结果,该研究利用氘化磷脂分子的氘(2H)核磁共振(NMR)以及固态13C和31P - NMR,研究了在不存在和存在胆固醇、麦角固醇和羊毛甾醇的情况下,磷脂酰胆碱(PC)双层膜的分子排列和动力学。使用在sn - 2链的2'、3'、4'、6'、8'、10'和12'位置特异性标记的二肉豆蔻酰磷脂酰胆碱(DMPC)以及全氘代的2 - [2H27]DMPC衍生物,在25℃下,对于DMPC、DMPC/胆固醇、DMPC/麦角固醇和DMPC/羊毛甾醇膜,在固定的甾醇/磷脂摩尔比为30%且存在过量水的情况下,确定了sn - 2链13个亚甲基中9个的排列轮廓。发现总体排列效应为麦角固醇>胆固醇>>羊毛甾醇。对这些体系的横向弛豫(T2e)研究表明,虽然对于DMPC、DMPC/胆固醇和DMPC/麦角固醇,相对弛豫率与假设双层分子协同运动为主要弛豫机制的模型在定性上一致,但DMPC/羊毛甾醇中的相对弛豫率异常高,表明脂质堆积发生了改变。使用在胆碱部分的三甲基铵基团处氘化的二棕榈酰磷脂酰胆碱(DPPC),我们发现甾醇在酰基链中诱导的差异排列和运动效应在凝胶相(Lβ)和液晶相中也反映在头基上。对这些体系的13C和1H自旋动力学研究,包括交叉极化、旋转框架纵向弛豫和偶极回波弛豫率,表明二元脂质体系中磷脂分子不同区域的流动性与甾醇诱导的排列效应呈负相关。C - D键序参数(通过2H - NMR获得)和13C - 1H交叉极化率的新组合证实了这些结果。相同摩尔比例的相同甾醇在25℃和35℃下对不饱和脂质1 - [2H31]棕榈酰 - 2 - 油酰 - sn - 甘油 - 3 - 磷脂酰胆碱(2H31 - POPC)的影响与在DMPC上观察到的不同,显示出胆固醇的排列效应最大,而麦角固醇和羊毛甾醇产生的效应明显较小。横向弛豫研究表明,虽然胆固醇不会扰乱POPC中的协同运动,但麦角固醇和羊毛甾醇会。同样,高分辨率固态13C - NMR研究支持了2H - NMR实验的结论。(摘要截断于400字)