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通过激光诱导荧光检测对磁性富集内吞细胞器进行细胞器内 pH 值测定。

Individual organelle pH determinations of magnetically enriched endocytic organelles via laser-induced fluorescence detection.

机构信息

University of Minnesota, Department of Chemistry, 207 Pleasant Street SE, Minneapolis, Minnesota 55455-0431, USA.

出版信息

Anal Chem. 2011 Oct 1;83(19):7331-9. doi: 10.1021/ac201196n. Epub 2011 Sep 12.

Abstract

The analysis of biotransformations that occur in lysosomes and other endocytic organelles is critical to studies on intracellular degradation, nutrient recycling, and lysosomal storage disorders. Such analyses require bioactive organelle preparations that are devoid of other contaminating organelles. Commonly used differential centrifugation techniques produce impure fractions and may not be compatible with microscale separation platforms. Density gradient centrifugation procedures reduce the level of impurities but may compromise bioactivity. Here we report on simple magnetic setup and a procedure that produce highly enriched bioactive organelles based on their magnetic capture as they traveled through open tubes. Following capture, in-line laser-induced fluorecence detection (LIF) determined for the first time the pH of each magnetically retained individual endocytic organelle. Unlike bulk measurements, this method was suitable to describe the distributions of pH values in endocytic organelles from L6 rat myoblasts treated with dextran-coated iron oxide nanoparticles (for magnetic retention) and fluorescein/TMRM-conjugated dextran (for pH measurements by LIF). Their individual pH values ranged from 4 to 6, which is typical of bioactive endocytic organelles. These analytical procedures are of high relevance to evaluate lysosomal-related degradation pathways in aging, storage disorders, and drug development.

摘要

分析溶酶体和其他内吞细胞器中发生的生物转化对于研究细胞内降解、营养物质回收和溶酶体贮积症至关重要。此类分析需要无其他污染细胞器的生物活性细胞器制剂。常用的差速离心技术会产生不纯的级分,并且可能与微尺度分离平台不兼容。密度梯度离心程序虽然降低了杂质水平,但可能会损害生物活性。在这里,我们报告了一种简单的磁体设置和一种程序,该程序可基于它们在穿过开放管时的磁捕获来产生高度富集的生物活性细胞器。捕获后,在线激光诱导荧光检测 (LIF) 首次确定了每个磁性保留的内吞细胞器的 pH 值。与批量测量不同,该方法适用于描述用葡聚糖包覆的氧化铁纳米颗粒(用于磁性保留)和荧光素/TMRM 缀合的葡聚糖(用于通过 LIF 进行 pH 值测量)处理的 L6 大鼠成肌细胞中的内吞细胞器中 pH 值的分布。它们的个体 pH 值范围从 4 到 6,这是生物活性内吞细胞器的典型特征。这些分析程序对于评估与衰老、储存障碍和药物开发相关的溶酶体相关降解途径具有重要意义。

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