Cobb Stuart R, Pitt Andrew
Division of Neuroscience & Biomedical Systems, Institute of Biomedical & Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK.
Expert Rev Proteomics. 2008 Jun;5(3):393-404. doi: 10.1586/14789450.5.3.393.
Synaptic plasticity is the dynamic regulation of the strength of synaptic communication between nerve cells. It is central to neuronal development as well as experience-dependent remodeling of the adult nervous system as occurs during memory formation. Aberrant forms of synaptic plasticity also accompany a variety of neurological and psychiatric diseases, and unraveling the biological basis of synaptic plasticity has been a major goal in neurobiology research. The biochemical and structural mechanisms underlying different forms of synaptic plasticity are complex, involving multiple signaling cascades, reconfigurations of structural proteins and the trafficking of synaptic proteins. As such, proteomics should be a valuable tool in dissecting the molecular events underlying normal and disease-related forms of plasticity. In fact, progress in this area has been disappointingly slow. We discuss the particular challenges associated with proteomic interrogation of synaptic plasticity processes and outline ways in which we believe proteomics may advance the field over the next few years. We pay particular attention to technical advances being made in small sample proteomics and the advent of proteomic imaging in studying brain plasticity.
突触可塑性是神经细胞之间突触通讯强度的动态调节。它对于神经元发育以及成年神经系统依赖经验的重塑(如在记忆形成过程中发生的那样)至关重要。异常形式的突触可塑性也伴随着多种神经和精神疾病,而阐明突触可塑性的生物学基础一直是神经生物学研究的主要目标。不同形式的突触可塑性背后的生化和结构机制很复杂,涉及多个信号级联、结构蛋白的重新配置以及突触蛋白的运输。因此,蛋白质组学应该是剖析正常和疾病相关可塑性形式背后分子事件的宝贵工具。事实上,该领域的进展一直令人失望地缓慢。我们讨论了与突触可塑性过程的蛋白质组学研究相关的特殊挑战,并概述了我们认为蛋白质组学在未来几年可能推动该领域发展的方式。我们特别关注小样本蛋白质组学的技术进展以及蛋白质组成像在研究脑可塑性方面的出现。