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通过单粒子追踪对表皮生长因子受体簇扩散的表征

Characterization of the diffusion of epidermal growth factor receptor clusters by single particle tracking.

作者信息

Boggara Mohan, Athmakuri Krishna, Srivastava Sunit, Cole Richard, Kane Ravi S

机构信息

Howard P. Isermann Department of Chemical and Biological Engineering & Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

出版信息

Biochim Biophys Acta. 2013 Feb;1828(2):419-26. doi: 10.1016/j.bbamem.2012.08.022. Epub 2012 Sep 4.

Abstract

A number of studies have shown that receptors of the epidermal growth factor receptor family (ErbBs) exist as higher-order oligomers (clusters) in cell membranes in addition to their monomeric and dimeric forms. Characterizing the lateral diffusion of such clusters may provide insights into their dynamics and help elucidate their functional relevance. To that end, we used single particle tracking to study the diffusion of clusters of the epidermal growth factor (EGF) receptor (EGFR; ErbB1) containing bound fluorescently-labeled ligand, EGF. EGFR clusters had a median diffusivity of 6.8×10(-11)cm(2)/s and were found to exhibit different modes of transport (immobile, simple, confined, and directed) similar to that previously reported for single EGFR molecules. Disruption of actin filaments increased the median diffusivity of EGFR clusters to 10.3×10(-11)cm(2)/s, while preserving the different modes of diffusion. Interestingly, disruption of microtubules rendered EGFR clusters nearly immobile. Our data suggests that microtubules may play an important role in the diffusion of EGFR clusters either directly or perhaps indirectly via other mechanisms. To our knowledge, this is the first report probing the effect of the cytoskeleton on the diffusion of EGFR clusters in the membranes of live cells.

摘要

多项研究表明,表皮生长因子受体家族(ErbBs)的受体除了以单体和二聚体形式存在外,还以高阶寡聚体(簇)的形式存在于细胞膜中。表征此类簇的横向扩散可能有助于深入了解其动力学,并有助于阐明其功能相关性。为此,我们使用单粒子追踪技术研究了含有结合荧光标记配体表皮生长因子(EGF)的表皮生长因子受体(EGFR;ErbB1)簇的扩散。EGFR簇的中位扩散系数为6.8×10(-11)cm(2)/s,并且发现其表现出与先前报道的单个EGFR分子类似的不同运输模式(固定、简单、受限和定向)。肌动蛋白丝的破坏将EGFR簇的中位扩散系数提高到10.3×10(-11)cm(2)/s,同时保留了不同的扩散模式。有趣的是,微管的破坏使EGFR簇几乎固定不动。我们的数据表明,微管可能直接或通过其他机制间接在EGFR簇的扩散中发挥重要作用。据我们所知,这是第一份探究细胞骨架对活细胞膜中EGFR簇扩散影响的报告。

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