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通过整合跨空间和时间的见解来理解神经发育中的泛素化。

Understanding ubiquitination in neurodevelopment by integrating insights across space and time.

作者信息

Ambrozkiewicz Mateusz C, Lorenz Sonja

机构信息

Institute of Cell Biology and Neurobiology, Research Group 'Proteostasis', Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, Berlin, Germany.

Max Planck Institute for Multidisciplinary Sciences, Research Group 'Ubiquitin Signaling Specificity', Am Fassberg 11, Göttingen, Germany.

出版信息

Nat Struct Mol Biol. 2025 Jan;32(1):14-22. doi: 10.1038/s41594-024-01422-3. Epub 2024 Dec 4.

Abstract

Ubiquitination regulates a myriad of eukaryotic signaling cascades by modifying substrate proteins, thereby determining their functions and fates. In this perspective, we discuss current challenges in investigating the ubiquitin system in the developing brain. We foster the concept that ubiquitination pathways are spatiotemporally regulated and tightly intertwined with molecular and cellular transitions during neurogenesis and neural circuit assembly. Focusing on the neurologically highly relevant class of homologous to E6AP C-terminus (HECT) ubiquitin ligases, we propose cross-disciplinary translational approaches bridging state-of-the-art cell biology, proteomics, biochemistry, structural biology and neuroscience to dissect ubiquitination in neurodevelopment and its specific perturbations in brain diseases. We highlight that a comprehensive understanding of ubiquitin signaling in the brain may reveal new horizons in basic neuroscience and clinical applications.

摘要

泛素化通过修饰底物蛋白来调节无数真核生物信号级联反应,从而决定其功能和命运。从这个角度出发,我们讨论了在发育中的大脑中研究泛素系统目前所面临的挑战。我们提出这样一个概念,即泛素化途径在时空上受到调控,并在神经发生和神经回路组装过程中与分子和细胞转变紧密交织。聚焦于与E6AP C末端同源(HECT)的泛素连接酶这一与神经学高度相关的类别,我们提出跨学科的转化方法,将最先进的细胞生物学、蛋白质组学、生物化学、结构生物学和神经科学结合起来,以剖析神经发育中的泛素化及其在脑部疾病中的特定扰动。我们强调,对大脑中泛素信号的全面理解可能会在基础神经科学和临床应用中揭示新的前景。

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