相互作用体
后脑
生物
前脑
蛋白质组学
细胞生物学
细胞骨架
塞普汀
细胞应激反应
神经科学
中枢神经系统
神经系统
基因
基因亚型
海马结构
生物途径
细胞室
计算生物学
线粒体
转运蛋白
亚细胞定位
凝集素
病态的
作者
Ahlam S. Soliman,Andrew Umstead,Tessa Grabinski,Nicholas M. Kanaan,Andy Lee,John Ryan,Jared Lamp,Irving E. Vega
摘要
Abstract EFhd2 is a conserved calcium‐binding protein that is highly expressed in the central nervous system. We have shown that EFhd2 interacts with tau protein, a key pathological hallmark in Alzheimer's disease and related dementias. However, EFhd2’s physiological and pathological functions in the brain are still poorly understood. To gain insights into its physiological function, we identified proteins that co‐immunoprecipitated with EFhd2 from mouse forebrain and hindbrain, using tandem mass spectrometry (MS). In addition, quantitative mass spectrometry was used to detect protein abundance changes due to the deletion of the Efhd2 gene in mouse forebrain and hindbrain regions. Our data show that mouse EFhd2 is associated with cytoskeleton components, vesicle trafficking modulators, cellular stress response‐regulating proteins, and metabolic proteins. Moreover, proteins associated with the cytoskeleton, vesicular transport, calcium signaling, stress response, and metabolic pathways showed differential abundance in Efhd2 (−/−) mice. This study presents, for the first time, an EFhd2 brain interactome that it is associated with different cellular and molecular processes. These findings will help prioritize further studies to investigate the mechanisms by which EFhd2 modulates these processes in physiological and pathological conditions of the nervous system. image
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