Bonev B, Morrow M R
Department of Physics, Memorial University of Newfoundland, St. John's, Canada.
Biophys J. 1996 Jun;70(6):2727-35. doi: 10.1016/S0006-3495(96)79842-9.
Deuterium nuclear magnetic resonance spectroscopy was used to study the thermotropic phase behavior of dilauroylphosphatidylcholine (DLPC) bilayers at pressures up to 221 MPa. Pressure was found to separate the liquid crystal to gel transition from the gel to ordered crystalline phase transition. The jump in chain order observed on cooling through the transition into the gel phase was found to be small and thus consistent with the trend in longer chain saturated diacyl phosphatidylcholines. On cooling, DLPC was observed to enter an unusual state above the transition into the gel phase. This unusual state displayed fluid-like conformational order but short transverse relaxation times. It was found to be much better pronounced and to span a broader temperature range at elevated pressure than at lower pressures. Transverse relaxation measurements of deuterons on the chain alpha-carbons revealed a substantial slowing of molecular motions within the temperature range of the unusual fluid phase. The observation of such a phase at high pressure appears to be consistent with recent reports of an unusual fluid phase, Lx, in DLPC at ambient pressure.
利用氘核磁共振光谱研究了二月桂酰磷脂酰胆碱(DLPC)双层膜在高达221 MPa压力下的热致相行为。发现压力将液晶到凝胶的转变与凝胶到有序结晶相的转变区分开来。通过冷却进入凝胶相时观察到的链序跳跃很小,因此与长链饱和二酰基磷脂酰胆碱的趋势一致。在冷却时,观察到DLPC在进入凝胶相转变温度以上进入一种异常状态。这种异常状态表现出类似流体的构象有序,但横向弛豫时间较短。发现与较低压力相比,在高压下这种异常状态更明显且跨越更宽的温度范围。对链α-碳上的氘进行横向弛豫测量表明,在异常流体相的温度范围内分子运动显著减慢。在高压下观察到这样一个相似乎与最近关于在常压下DLPC中存在异常流体相Lx的报道一致。