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同步膜电容测量与全内反射荧光显微镜技术用于研究免疫突触处的颗粒运输

Simultaneous Membrane Capacitance Measurements and TIRF Microscopy to Study Granule Trafficking at Immune Synapses.

作者信息

Sleiman Marwa, Stevens David R, Rettig Jens

机构信息

Center for Integrative Physiology and Molecular Medicine, Universität des Saarlandes, Building 48, Homburg/Saar, 66421, Germany.

出版信息

Methods Mol Biol. 2017;1584:157-169. doi: 10.1007/978-1-4939-6881-7_11.

Abstract

Whole-cell capacitance measurements allow the direct measurement of exocytosis with high temporal resolution. An added benefit of the whole-cell configuration is the possibility to control the cytosolic free calcium concentration allowing examination of the role of intracellular calcium in a variety of processes. We have coupled this method with imaging of cytotoxic granule release using total internal reflection fluorescence microscopy (TIRFM) to identify the capacitance steps associated with cytotoxic granule release identified by TIRFM. This requires the use of fluorescent granule markers to identify cytotoxic granules and allows characterization of cytotoxic granule fusion and of the behavior of cytotoxic granules at the immune synapse prior to fusion. Combination of these methods enables the study of a number of processes relevant to the function of the immune synapse.

摘要

全细胞电容测量能够以高时间分辨率直接测量胞吐作用。全细胞配置的一个额外优势是可以控制胞质游离钙浓度,从而能够研究细胞内钙在各种过程中的作用。我们已将此方法与使用全内反射荧光显微镜(TIRFM)对细胞毒性颗粒释放进行成像相结合,以识别与TIRFM所确定的细胞毒性颗粒释放相关的电容变化步骤。这需要使用荧光颗粒标记物来识别细胞毒性颗粒,并能够对细胞毒性颗粒融合以及融合前免疫突触处细胞毒性颗粒的行为进行表征。这些方法的结合使得能够研究许多与免疫突触功能相关的过程。

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