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.
Sci Rep. 2017 Dec 1;7(1):16801. doi: 10.1038/s41598-017-16361-x.
Imaging the distribution of sphingomyelin (SM) in membranes is an important issue in lipid-raft research. Recently we developed novel fluorescent SM analogs that exhibit partition and dynamic behaviors similar to native SM, and succeeded in visualizing lateral domain-segregation between SM-rich liquid-ordered (L) and SM-poor liquid-disordered (L) domains. However, because the fluorescent contrast between these two domains depends directly on their partition ratio for the fluorescent SMs, domain-separation becomes indeterminate when the distribution difference is not great enough. In this study, we propose the use of inter-lipid Förster resonance energy transfer (FRET) imaging between fluorescent SMs to enhance the contrast of the two domains in cases in which the inter-domain difference in SM distribution is inadequate for conventional monochromic imaging. Our results demonstrate that inter-lipid FRET intensity was significantly higher in the L domain than in the L domain, resulting in a clear and distinguishable contrast between the two domains even in poorly phase-separated giant unilamellar vesicles. In addition, we show that inter-lipid FRET imaging is useful for selective visualization of highly condensed assemblies and/or clusters of SM molecules in living cell membranes. Thus, the inter-lipid FRET imaging technique can selectively emphasize the SM-condensed domains in both artificial and biological membranes.
在脂质筏研究中,对鞘磷脂(SM)在膜中分布的成像一直是一个重要的问题。最近,我们开发了新型荧光 SM 类似物,其分配和动态行为与天然 SM 相似,并成功地可视化了富含 SM 的液相有序(L)和 SM 贫液相无序(L)域之间的侧向域分离。然而,由于这两个域之间的荧光对比度直接取决于它们对荧光 SM 的分配比例,因此当分配差异不够大时,域分离变得不确定。在这项研究中,我们提出使用荧光 SM 之间的脂质间Förster 共振能量转移(FRET)成像来增强两个域的对比度,当 SM 分布的域间差异不足以用于常规单色成像时,这种方法非常有效。我们的结果表明,脂质间 FRET 强度在 L 域中显著高于 L 域,即使在相分离较差的巨大单层囊泡中,也能在两个域之间产生清晰且可区分的对比度。此外,我们表明脂质间 FRET 成像可用于选择性地可视化活细胞膜中 SM 凝聚组装体和/或簇的高分辨率。因此,脂质间 FRET 成像技术可以选择性地强调人工和生物膜中 SM 凝聚的域。