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用于研究长期记忆背后分子机制的从头蛋白质组学方法。

De novo proteomic methods for examining the molecular mechanisms underpinning long-term memory.

作者信息

Evans Harrison Tudor, Blackmore Daniel, Götz Jürgen, Bodea Liviu-Gabriel

机构信息

Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane QLD 4072, Australia.

Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane QLD 4072, Australia.

出版信息

Brain Res Bull. 2021 Apr;169:94-103. doi: 10.1016/j.brainresbull.2020.12.015. Epub 2021 Jan 16.

Abstract

Memory formation is a fundamental function of the nervous system that enables the experience-based adaptation of behaviour. The formation, recall and updating of long-term memory (LTM) requires new protein synthesis through its direct involvement in neuronal processes, such as long-term potentiation (LTP), long-term depression (LTD) and synaptic scaling. We discuss the advantages and limitations of several emerging techniques which enable the tagging of newly synthesised proteins, including stable isotope labelling with amino acids in cell culture (SILAC), puromycin labelling, and non-canonical amino acid (NCAA) labelling. We further present how these methods allow for the identification and visualisation of proteins which are newly synthesised during different stages of memory formation. These emerging techniques will continue to expand our understanding of how memories are formed, consolidated and retrieved.

摘要

记忆形成是神经系统的一项基本功能,它使行为能够基于经验进行适应性调整。长期记忆(LTM)的形成、回忆和更新需要通过直接参与神经元过程(如长时程增强(LTP)、长时程抑制(LTD)和突触缩放)来合成新的蛋白质。我们讨论了几种新兴技术的优点和局限性,这些技术能够对新合成的蛋白质进行标记,包括细胞培养中氨基酸的稳定同位素标记(SILAC)、嘌呤霉素标记和非标准氨基酸(NCAA)标记。我们还介绍了这些方法如何用于识别和可视化在记忆形成的不同阶段新合成的蛋白质。这些新兴技术将继续拓展我们对记忆如何形成、巩固和提取的理解。

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