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Non-destructive handling of individual chromatin fibers isolated from single cells in a microfluidic device utilizing an optically driven microtool

机译:使用光学驱动的微型工具在微流控设备中无损处理从单个细胞分离的单个染色质纤维

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We report a novel method for the non-destructive handling of, and biochemical experiments with, individual intact chromatin fibers, as well as their isolation from single cells, utilizing a specifically designed microfluidic device with an optically driven microtool under the microscope. Spheroplasts of recombinant fission yeast cells expressing fluorescent protein-tagged core histones were employed, and isolation of chromatin fibers was conducted by cell bursting via changing from isotonic conditions to hypotonic conditions in the microfluidic device. The isolation of chromatin fibers was confirmed by the fluorescent protein-tagged core histones involved in the chromatin fibers. For the non-destructive handling of the isolated chromatin fibers in the microfluidic device, we developed antibody-conjugated microspheres, which had affinity to the fluorescent protein-tagged core histones, and the microspheres were manipulated using optical tweezers, which functioned as optically driven microtools. With the aid of the microtool, isolated chromatin fibers were handled non-destructively and were tethered at the microstructures fabricated in the microfluidic device with straightened conformation by the flow. Immunofluorescence staining was carried out as a demonstrative biochemical experiment with the individual native chromatin fibers isolated in the microfluidic device, and specific fluorescent spots were visualized along the tethered chromatin fibers. Thus, the potential application of this method for epigenetic analyses of intact chromatin fibers isolated from single cells is demonstrated.
机译:我们报告了一种新颖的方法,用于对单个完整染色质纤维进行无损处理和生化实验,以及将它们从单个细胞中分离出来,利用特别设计的微流控设备以及在显微镜下的光学驱动微工具。使用表达荧光蛋白标记的核心组蛋白的重组裂变酵母细胞的原生质体,并通过在微流体装置中从等渗条件变为低渗条件,通过细胞破裂来分离染色质纤维。染色质纤维的分离是通过染色质纤维中涉及的荧光蛋白标记的核心组蛋白来证实的。为了在微流控设备中对分离的染色质纤维进行非破坏性处理,我们开发了与抗体偶联的微球,该微球对带有荧光蛋白标签的核心组蛋白具有亲和力,并且使用光学镊子操纵了微球,该镊子起着光学驱动的微型工具的作用。借助于微工具,分离的染色质纤维被无损地处理,并被束缚在微流体装置中制造的微结构上,并通过流动被拉直。免疫荧光染色是作为示范性生化实验,使用微流控设备中分离出的各个天然染色质纤维进行染色,沿束缚的染色质纤维可视化了特定的荧光斑点。因此,证明了该方法在从单个细胞分离的完整染色质纤维的表观遗传分析中的潜在应用。

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