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使用共聚焦显微镜对细胞连接蛋白进行时空定位。

Spatial and Temporal Localization of Connexins in Cells Using Confocal Microscopy.

机构信息

Department of Anatomy and Cell Biology, University of Western Ontario, London, ON, Canada.

Department of Physiology and Pharmacology, University of Western Ontario, London, ON, Canada.

出版信息

Methods Mol Biol. 2024;2801:57-74. doi: 10.1007/978-1-0716-3842-2_5.

Abstract

The 21-member connexin family found in humans is the building block of both single-membrane spanning channels (hemichannels) and double-membrane spanning intercellular channels. These large-pore channels are dynamic and typically have a short life span of only a few hours. Imaging connexins from the time of synthesis in the endoplasmic reticulum through to their degradation can be challenging given their distinct assembly states and transient residences in many subcellular compartments. Here, we describe how connexins can be effectively imaged on a confocal microscope in living cells when tagged with fluorescent proteins and when immunolabeled with high affinity anti-connexin antibodies in fixed cells. Temporal and spatial localization of multiple connexins and disease-linked connexin mutants at the subcellular level extensively informs on the mechanisms governing connexin regulation in health and disease.

摘要

在人类中发现的 21 个连接子家族是单膜跨越通道(半通道)和双膜跨越细胞间通道的构建块。这些大孔通道是动态的,通常只有几个小时的短暂寿命。鉴于其独特的组装状态和在许多亚细胞隔室中的短暂居留,从内质网中连接子的合成时间到它们的降解时间进行成像可能具有挑战性。在这里,我们描述了当用荧光蛋白标记和在固定细胞中用高亲和力抗连接子抗体免疫标记时,如何在活细胞中的共聚焦显微镜上有效地对连接子进行成像。在亚细胞水平上对多个连接子和与疾病相关的连接子突变体的时间和空间定位,广泛地说明了在健康和疾病中调节连接子的机制。

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