INSERM U862, Neurocenter Magendie, Pathophysiology of Addiction group, Bordeaux F33077, France.
J Neurosci Methods. 2011 Jun 15;198(2):204-12. doi: 10.1016/j.jneumeth.2011.04.001. Epub 2011 Apr 12.
The Central Nervous System (CNS) is constituted of complex and specific anatomical regions that cluster together and interact with each other with the ultimate objective of receiving and delivering information. This information is characterized by selective biochemical changes that happen within specific brain sub-regions. Most of these changes involve a dynamic balance between kinase and phosphatase activities. The fine-tuning of this kinase/phosphatase balance is thus critical for neuronal adaptation, transition to long-term responses and higher brain functions including specific behaviors. Data emerging from several biological systems may suggest that disruption of this dynamic cell signaling balance within specific brain sub-regions leads to behavioral impairments. Therefore, accurate and powerful techniques are required to study global changes in protein expression levels and protein activities in specific groups of cells. Laser-based systems for tissue microdissection represent a method of choice enabling more accurate proteomic profiling. The goal of this study was to develop a methodological approach using Laser Microdissection and Pressure Catapulting (LMPC) technology combined with an immunoblotting technique in order to specifically detect the expression of phosphoproteins in particular small brain areas.
中枢神经系统(CNS)由复杂且特定的解剖区域构成,这些区域聚集在一起并相互作用,最终目的是接收和传递信息。这些信息的特征是在特定的脑区发生选择性的生化变化。这些变化大多数涉及激酶和磷酸酶活性之间的动态平衡。因此,这种激酶/磷酸酶平衡的微调对于神经元适应、向长期反应和包括特定行为在内的更高脑功能的转变至关重要。来自几个生物系统的数据可能表明,特定脑区中这种动态细胞信号平衡的破坏会导致行为障碍。因此,需要准确而强大的技术来研究特定细胞群中蛋白质表达水平和蛋白质活性的全局变化。基于激光的组织微切割系统是一种可行的选择方法,可以实现更精确的蛋白质组学分析。本研究的目的是开发一种使用激光微切割和压力弹射(LMPC)技术与免疫印迹技术相结合的方法,以便特异性地检测特定小脑区中磷酸蛋白的表达。