Lipid-Protein Microinclusions in the Morphological Structures of Organelle Membranes Studied by Fluorescent Confocal Microscopy

M. Chernyshov, V. Nurminsky, N. V. Ozolina
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引用次数: 2

Abstract

Peculiar properties of morphological structures of organelle membranes were studied by fluorescent confocal microscopy. The list of objects in our experiments was represented by mitochondria, chloroplasts and vacuoles. During this study, identification of lipid microinclusions having the form of such lipid-protein structural microformations as lipid-protein microdomains, vesicles and membrane tubular structures (cytoplasmic transvacuolar strands and nanotubes) located in organelle membranes or bound up with them was conducted. Such membrane probes as laurdan, DPH, ANS and bis-ANS were used. Comparison of fluorescence intensity of these membrane probes was conducted. This investigation of the morphological properties of lipid-protein structural microformations was accompanied with analysis of 1) the phase state and 2) dynamics of microviscosity variations in the membrane elements of isolated plant cell organelles. Distributions of laurdan fluorescence generalized polarization (GP) values for the membrane on the whole and for the intensively fluorescing membrane segments were obtained. It was discovered that the microviscosity of intensively fluorescing membrane segments essentially differed from the microviscosity of the rest part of the membrane. In conclusion, some results of the study of peculiar properties of lipid-protein structural microformations related to the structure of organelle membranes and the discoveries made in this investigation are discussed.
荧光共聚焦显微镜研究细胞器膜形态结构中的脂质蛋白微包裹体
用荧光共聚焦显微镜研究了细胞器膜形态结构的特殊性质。我们的实验对象以线粒体、叶绿体和液泡为代表。在本研究中,鉴定了具有脂质-蛋白质结构微结构形式的脂质微内含物,如脂质-蛋白质微结构域、囊泡和膜管结构(细胞质跨液泡链和纳米管),这些结构位于细胞器膜上或与它们结合。采用laurdan、DPH、ANS、bis-ANS等膜探针。比较了这两种膜探针的荧光强度。对脂质-蛋白结构微形成形态特性的研究伴随着对分离植物细胞器膜元件的相态和微粘度变化动力学的分析。得到了膜整体和强荧光膜段的laurdan荧光广义偏振(GP)值的分布。研究发现,荧光强烈的膜段的微粘度与膜其余部分的微粘度有本质的不同。最后,讨论了与细胞器膜结构有关的脂质-蛋白结构微形成特性的一些研究结果和本研究的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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