Degani H, Danon A, Caplan S R
Biochemistry. 1980 Apr 15;19(8):1626-31. doi: 10.1021/bi00549a016.
The thermotropic behavior and the dynamic properties of the polar lipids of Halobacterium halobium were studied by 1H and 13C NMR. The studies were performed on three different preparations: micellar solutions in deuterated chloroform, multilamellar dispersions in 2H2O, and unilamellar vesicles obtained from the latter by ultrasonication. Due to the methyl side groups in the alkyl chains of these lipids, the 13C spectra are highly resolved in particular in the micellar solution, allowing peak assignment of the alkyl chain carbons. Proton and 13C T1 relaxation and line width measurements were made for all three preparations. In both lamellar dispersions, sharp discontinuities in these parameters were observed around 35 degrees C. This behavior is attributed to an abrupt change in the dynamics of the lipids within the membrane. The variation of the specific relaxation rate 1/NT1 of the 13C nuclei along the hydrocarbon chains of the H. halobium lipids exhibits maxima at the tertiary carbons to which the methyl side groups are attached. These maxima are particularly pronounced in the lamellar phases and suggest that the segmental motion ("kink" formation) at the tertiary carbons is hindered by the presence of the methyl groups.
通过1H和13C核磁共振研究了嗜盐嗜盐菌极性脂质的热致行为和动态特性。研究针对三种不同制剂进行:氘代氯仿中的胶束溶液、重水(2H2O)中的多层分散体以及通过超声处理从后者获得的单层囊泡。由于这些脂质的烷基链中存在甲基侧基,13C谱在胶束溶液中尤其高度分辨,从而能够对烷基链碳进行峰归属。对所有三种制剂进行了质子和13C T1弛豫及线宽测量。在两种层状分散体中,在约35℃处观察到这些参数的急剧不连续性。这种行为归因于膜内脂质动力学的突然变化。嗜盐嗜盐菌脂质烃链上13C核的比弛豫率1/NT1的变化在连接甲基侧基的叔碳处呈现最大值。这些最大值在层状相中尤为明显,表明叔碳处的链段运动(“扭结”形成)受到甲基存在的阻碍。