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首页> 外文期刊>Zoological Science >Single-Cell Electroporation of Fluorescent Probes into Sea Urchin Sperm Cells and Subsequent FRAP Analysis
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Single-Cell Electroporation of Fluorescent Probes into Sea Urchin Sperm Cells and Subsequent FRAP Analysis

机译:荧光探针的单细胞电穿孔进入海胆精子细胞并进行随后的FRAP分析

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摘要

In sea urchin spermatozoa, the energy required for flagellar motility depends only on the diffusional supply from proximal mitochondria, and thus the diffusion rate inside flagella is one of the most crucial factors limiting the practical size and design of the motile machinery. To determine the diffusion rates of materials inside sperm cells, FRAP (fluorescence recovery after photobleaching) analysis of incorporated fluorescent probes is one of the most powerful approaches. However, the only practically possible method until now was to use the ester forms of fluorescence, and our choice was limited to those of relatively small molecular masses, such as fluorescein derivatives. In this report, we show that a modified single-cell electroporation technique can be applied as a new microinjection method for sperm cells of the sea urchin. The method was applied to FRAP analysis to determine the rate of intraflagellar diffusion.
机译:在海胆精子中,鞭毛运动所需的能量仅取决于来自近端线粒体的扩散供应,因此,鞭毛内部的扩散速率是限制活动装置的实际尺寸和设计的最关键因素之一。为了确定精子细胞内物质的扩散速率,结合荧光探针的FRAP(光漂白后的荧光恢复)分析是最有效的方法之一。但是,到目前为止,实际上唯一可行的方法是使用荧光的酯形式,而我们的选择仅限于分子量相对较小的那些形式,例如荧光素衍生物。在此报告中,我们表明,改良的单细胞电穿孔技术可以用作海胆精子细胞的新显微注射方法。该方法应用于FRAP分析,以确定鞭毛内扩散的速率。

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