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突触的神经蛋白质组学:蛋白质网络和信号转导的亚细胞定量。

Neuroproteomics of the Synapse: Subcellular Quantification of Protein Networks and Signaling Dynamics.

机构信息

Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands; Netherlands Proteomics Center, Utrecht, The Netherlands.

Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands; Netherlands Proteomics Center, Utrecht, The Netherlands.

出版信息

Mol Cell Proteomics. 2021;20:100087. doi: 10.1016/j.mcpro.2021.100087. Epub 2021 Apr 29.

DOI:10.1016/j.mcpro.2021.100087
PMID:33933679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8167277/
Abstract

One of the most fascinating features of the brain is its ability to adapt to its surroundings. Synaptic plasticity, the dynamic mechanism of functional and structural alterations in synaptic strength, is essential for brain functioning and underlies a variety of processes such as learning and memory. Although the molecular mechanisms underlying such rapid plasticity are not fully understood, a consensus exists on the important role of proteins. The study of these neuronal proteins using neuroproteomics has increased rapidly in the last decades, and advancements in MS-based proteomics have broadened our understanding of neuroplasticity exponentially. In this review, we discuss the trends in MS-based neuroproteomics for the study of synaptic protein-protein interactions and protein signaling dynamics, with a focus on sample types, different labeling and enrichment approaches, and data analysis and interpretation. We highlight studies from the last 5 years, with a focus on synapse structure, composition, functioning, or signaling and finally discuss some recent developments that could further advance the field of neuroproteomics.

摘要

大脑最迷人的特征之一是其适应周围环境的能力。突触可塑性是突触强度功能和结构改变的动态机制,对于大脑功能至关重要,是多种过程(如学习和记忆)的基础。尽管尚不完全了解这种快速可塑性的分子机制,但人们普遍认为蛋白质起着重要作用。过去几十年中,使用神经蛋白质组学研究这些神经元蛋白的数量迅速增加,基于 MS 的蛋白质组学的进步使我们对神经可塑性的理解呈指数级增长。在这篇综述中,我们讨论了基于 MS 的神经蛋白质组学在研究突触蛋白-蛋白相互作用和蛋白信号动力学方面的趋势,重点介绍了不同的样本类型、标记和富集方法以及数据分析和解释。我们强调了过去 5 年来的一些研究,重点是突触结构、组成、功能或信号转导,最后讨论了一些可能进一步推动神经蛋白质组学领域发展的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/8f7482fc1aca/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/d1df309dbe2e/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/ecbbe1c9a79d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/98bd12b9f5bc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/3f1a03d253d2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/8f7482fc1aca/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/d1df309dbe2e/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/ecbbe1c9a79d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/98bd12b9f5bc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/3f1a03d253d2/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d3/8167277/8f7482fc1aca/gr4.jpg

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