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基于拉曼显微镜的细胞内脂物理性质定量分析。

Raman microscopy-based quantification of the physical properties of intracellular lipids.

机构信息

Department of Lipid Signaling, National Center for Global Health and Medicine, 1-21-1 Toyama, Shinjuku-ku, Tokyo, Japan.

Department of Lipidomics, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan.

出版信息

Commun Biol. 2021 Oct 8;4(1):1176. doi: 10.1038/s42003-021-02679-w.

Abstract

The physical properties of lipids, such as viscosity, are homeostatically maintained in cells and are intimately involved in physiological roles. Measurement of the physical properties of plasma membranes has been achieved primarily through chemical or genetically encoded fluorescent probes. However, since most probes target plasma membranes, physical properties of lipids in intracellular organelles, including lipid droplets (LDs) are yet to be analyzed. Here, we present a novel Raman microscopy-based approach for quantifying the physical properties of intracellular lipids under deuterium-labeled fatty acid treatment conditions. Focusing on the fact that Raman spectra of carbon-deuterium vibration are altered depending on the surrounding lipid species, we quantitatively represented the physical properties of lipids as the gauche/trans conformational ratio of the introduced labeled fatty acids, which can be used as an indicator of viscosity. Intracellular Raman imaging revealed that the gauche/trans ratio of cytosolic regions was robustly preserved against perturbations attempting to alter the lipid composition. This was likely due to LDs functioning as a buffer against excess gauche/trans ratio, beyond its traditional role as an energy storage organelle. Our novel approach enables the observation of the physical properties of organelle lipids, which is difficult to perform with conventional probes, and is useful for quantitative assessment of the subcellular lipid environment.

摘要

脂质的物理性质,如黏度,在细胞中是维持内稳态的,并密切参与生理作用。血浆膜的物理性质的测量主要通过化学或遗传编码的荧光探针来实现。然而,由于大多数探针针对的是质膜,因此包括脂滴(LDs)在内的细胞内细胞器中的脂质的物理性质尚未得到分析。在这里,我们提出了一种新的基于拉曼显微镜的方法,用于在氘标记脂肪酸处理条件下定量分析细胞内脂质的物理性质。我们专注于这样一个事实,即碳-氘振动的拉曼光谱根据周围的脂质种类而改变,我们将引入的标记脂肪酸的物理性质定量表示为其 gauche/trans 构象比,该比可以用作粘度的指标。细胞内拉曼成像显示,细胞质区域的 gauche/trans 比在试图改变脂质组成的干扰下得到了稳健的保持。这可能是由于 LD 作为缓冲液发挥作用,以防止 gauche/trans 比过度增加,超出其作为能量储存细胞器的传统作用。我们的新方法使我们能够观察细胞器脂质的物理性质,这是常规探针难以实现的,并且对亚细胞脂质环境的定量评估很有用。

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