Kinoshita Masanao, Matsumori Nobuaki, Murata Michio
JST ERATO, Lipid Active Structure Project, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan; Project Research Center for Fundamental Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.
JST ERATO, Lipid Active Structure Project, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan; Department of Chemistry, Graduate School of Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.
Biochim Biophys Acta. 2014 May;1838(5):1372-81. doi: 10.1016/j.bbamem.2014.01.017. Epub 2014 Jan 24.
Recently, DHSM, a minor constituent in naturally occurring SMs, was indicated to form a raft-like ordered phase more effectively than a naturally occurring form of SM because DHSM has greater potential to induce the intermolecular hydrogen bond. In order to examine the influence of the DHSM-induced hydrogen bond on the phase segregation, the thermal phase behavior of stearoyl-DHSM/DOPC binary bilayers was examined using calorimetry and fluorescence observation and compared with that of SSM/DOPC binary bilayers. Results revealed that the DHSM/DOPC bilayers undergo phase segregation between two L(α) phases within a limited compositional range. On the other hand, apparent phase separation was not observed above main transition temperature in SSM/DOPC mixtures. Our monolayer measurements showed that the lipid packing of DHSM is less perturbed than that of SSM by the addition of small amount of DOPC, indicating a stronger hydrogen bond between DHSM molecules. Therefore, in DHSM/DOPC binary bilayers, DHSM molecules may locally accumulate to form a DHSM-rich domain due to a DHSM-induced hydrogen bond. On the other hand, excess accumulation of DHSM should be prevented because the difference in the curvature between DHSM and DOPC assemblies causes elastic constraint at the domain boundary between the DHSM-rich and DOPC-rich domains. Competition between the energetic advantages provided by formation of the hydrogen bond and the energetic disadvantage conferred by elastic constraints likely results in L(α)/L(α) phase separation within a limited compositional range.
最近,DHSM作为天然存在的鞘脂(SMs)中的一种次要成分,被指出比天然形式的SM更有效地形成筏状有序相,因为DHSM具有更大的潜力诱导分子间氢键。为了研究DHSM诱导的氢键对相分离的影响,使用量热法和荧光观察研究了硬脂酰-DHSM/DOPC二元双层膜的热相行为,并与SSM/DOPC二元双层膜进行了比较。结果表明,DHSM/DOPC双层膜在有限的组成范围内经历两个L(α)相之间的相分离。另一方面,在SSM/DOPC混合物的主转变温度以上未观察到明显的相分离。我们的单层测量表明,添加少量DOPC时,DHSM的脂质堆积比SSM受到的扰动更小,这表明DHSM分子之间的氢键更强。因此,在DHSM/DOPC二元双层膜中,由于DHSM诱导的氢键,DHSM分子可能会局部聚集形成富含DHSM的区域。另一方面,应防止DHSM的过度积累,因为DHSM和DOPC组装体之间的曲率差异会在富含DHSM和富含DOPC的区域之间的域边界处产生弹性约束。氢键形成所提供的能量优势与弹性约束所带来的能量劣势之间的竞争可能导致在有限的组成范围内出现L(α)/L(α)相分离。