Dieterich Daniela C, Kreutz Michael R
From the ‡Institute for Pharmacology and Toxicology, Otto-von-Guericke University Magdeburg, Germany; Research Group Neuralomics, Leibniz Institute for Neurobiology Magdeburg, Germany; ¶Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany.
§RG Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany; ¶Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany.
Mol Cell Proteomics. 2016 Feb;15(2):368-81. doi: 10.1074/mcp.R115.051482. Epub 2015 Aug 25.
The advances in mass spectrometry based proteomics in the past 15 years have contributed to a deeper appreciation of protein networks and the composition of functional synaptic protein complexes. However, research on protein dynamics underlying core mechanisms of synaptic plasticity in brain lag far behind. In this review, we provide a synopsis on proteomic research addressing various aspects of synaptic function. We discuss the major topics in the study of protein dynamics of the chemical synapse and the limitations of current methodology. We highlight recent developments and the future importance of multidimensional proteomics and metabolic labeling. Finally, emphasis is given on the conceptual framework of modern proteomics and its current shortcomings in the quest to gain a deeper understanding of synaptic plasticity.
过去15年中,基于质谱的蛋白质组学进展使人们对蛋白质网络和功能性突触蛋白复合物的组成有了更深入的认识。然而,关于大脑中突触可塑性核心机制背后的蛋白质动力学研究却远远滞后。在本综述中,我们概述了针对突触功能各个方面的蛋白质组学研究。我们讨论了化学突触蛋白质动力学研究中的主要课题以及当前方法的局限性。我们强调了多维蛋白质组学和代谢标记的最新进展及其未来的重要性。最后,重点阐述了现代蛋白质组学的概念框架及其在深入理解突触可塑性方面目前存在的不足。