Peng X, Jonas A, Jonas J
Department of Chemistry, School of Chemical Sciences, University of Illinois, Urbana 61801, USA.
Biophys J. 1995 Mar;68(3):1137-44. doi: 10.1016/S0006-3495(95)80288-2.
High pressure 2H multipulse NMR techniques were used to investigate the effects of pressure on the structure and dynamics of selectively deuterated 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) multilamellar aqueous dispersions. The samples were deuterated on both chains at positions 2, 9, or 13. The deuterium lineshapes, the spin-lattice relaxation times, T1, and the spin-spin relaxation times, T2, were measured as a function of pressure from 1 bar to 5 kbar at 50 degrees C for the three deuterated DPPC samples. This pressure range permitted us to explore the phase behavior of DPPC from the liquid-crystalline (LC) phase through various gel phases such as the Gel I (P beta), Gel II (L beta), Gel III, Gel X, and the interdigitated, Gel i, gel phase. Pressure had an ordering effect on all chain segments both in the LC phase and various high pressure gel phases as indicated by the increase in SCD bond order parameter and the first moment, M1, with pressure. Compared with the adjacent gel phases, the Gel i phase had the highest order. Also, in all gel phases the carbon-9 segment of the chains had the most restricted motions in contrast to the LC phase, where the carbon-2 segment was the most restricted. In the LC phase, T1 and T2 values for all segments decreased with pressure, indicative of the fast correlation time regime. Similarly, T1 decreased with pressure in the Gel I and the interdigitated Gel i gel phases but changed to the slow correlation time regime at the Gel i/Gel II phase transition. For T2, which reflects slow motions, the transition to the slow correlation time regime occurred already at LC/Gel I phase transition. Considering the various motions which contribute to relaxation, the behavior of T1 and T2 in the Gel 11 through Gel X phases showing discontinuities and slope changes at the phase transitions was, as expected, quite complex.In addition we found a straight line relationship for T-1 vs. S2D, and T-1 vs. S2CD for the deuterons in the 9 and 13 positions in the LC phase in the pressure range investigated.
采用高压2H多脉冲核磁共振技术研究了压力对选择性氘代的1,2 - 二棕榈酰 - sn - 甘油 - 3 - 磷酸胆碱(DPPC)多层水分散体系结构和动力学的影响。样品在两条链的2、9或13位进行了氘代。在50℃下,对三个氘代DPPC样品测量了从1巴到5千巴压力范围内的氘线形、自旋 - 晶格弛豫时间T1和自旋 - 自旋弛豫时间T2。该压力范围使我们能够探究DPPC从液晶(LC)相到各种凝胶相的相行为,如凝胶I(Pβ)、凝胶II(Lβ)、凝胶III、凝胶X以及交错的凝胶i相。如SCD键序参数和一阶矩M1随压力增加所示,压力对LC相和各种高压凝胶相中的所有链段都有有序化作用。与相邻的凝胶相相比,凝胶i相具有最高的有序度。此外,在所有凝胶相中,链的碳 - 9段的运动受限最大,而在LC相中碳 - 2段的运动受限最大。在LC相中,所有链段的T1和T2值随压力降低,表明处于快速相关时间区域。类似地,在凝胶I和交错的凝胶i相中T1随压力降低,但在凝胶i/凝胶II相转变时转变为慢相关时间区域。对于反映慢运动的T2,在LC/凝胶I相转变时就已转变为慢相关时间区域。考虑到对弛豫有贡献的各种运动,T1和T2在凝胶II到凝胶X相中的行为在相变处显示出不连续性和斜率变化,正如预期的那样相当复杂。此外,在所研究的压力范围内,我们发现LC相中9位和13位氘核的T1与S2D以及T1与S2CD之间存在直线关系。