Department of Neurobiology and Anatomy, University of Texas Medical School, Houston, TX 77030, USA.
Neuroscience. 2010 Feb 17;165(4):1182-90. doi: 10.1016/j.neuroscience.2009.11.066. Epub 2009 Dec 1.
Post-translational modifications of proteins are a major determinant of biological function. Phosphorylation of proteins involved in signal transduction contributes to the induction and maintenance of several examples of cellular and synaptic plasticity. In this study we have identified phosphoproteins regulated by Pavlovian conditioning in lysates of Hermissenda nervous systems using two-dimensional electrophoresis (2DE) in conjunction with (32)P labeling, fluorescence based phosphoprotein in-gel staining, and mass spectrometry. Modification of protein phosphorylation regulated by conditioning was first assessed by densitometric analysis of (32)P labeled proteins resolved by 2DE from lysates of conditioned and pseudorandom control nervous systems. An independent assessment of phosphorylation regulated by conditioning was obtained from an examination of 2D gels stained with Pro-Q Diamond phosphoprotein dye. Mass spectrometric analysis of protein digests from phosphoprotein stained analytical gels or Coomassie Blue stained preparative gels provided for the identification of phosphoproteins that exhibited statistically significant increased phosphorylation in conditioned groups as compared to pseudorandom controls. A previously identified cytoskeletal related protein, Csp24 (24 kDa conditioned stimulus pathway phosphoprotein), involved in intermediate-term memory exhibited significantly increased phosphorylation detected 24 h post-conditioning. Our results show that proteins involved in diverse cellular functions such as transcriptional regulation, cell signaling, cytoskeletal regulation, metabolic activity, and protein degradation contribute to long-term post-translational modifications associated with Pavlovian conditioning.
蛋白质的翻译后修饰是生物功能的主要决定因素。参与信号转导的蛋白质的磷酸化有助于诱导和维持几种细胞和突触可塑性的例子。在这项研究中,我们使用二维电泳(2DE)结合(32)P 标记、基于荧光的磷酸蛋白胶内染色和质谱法,在 Hermissenda 神经系统的裂解物中鉴定了受巴甫洛夫条件作用调节的磷酸蛋白。通过 2DE 从条件和伪随机对照神经系统的裂解物中分离出(32)P 标记的蛋白质进行密度计分析,首先评估了由条件作用调节的蛋白质磷酸化修饰。从用 Pro-Q Diamond 磷酸蛋白染料染色的 2D 凝胶进行的磷酸化调节的独立评估,从磷酸蛋白染色的分析凝胶或考马斯亮蓝染色的制备凝胶的蛋白质消化物的质谱分析提供了用于鉴定在条件组中与伪随机对照相比表现出统计学上显著增加磷酸化的磷酸蛋白。先前鉴定的与细胞骨架相关的蛋白质 Csp24(24 kDa 条件刺激途径磷酸蛋白),参与中期记忆,在条件后 24 小时检测到明显增加的磷酸化。我们的结果表明,参与转录调节、细胞信号转导、细胞骨架调节、代谢活性和蛋白质降解等多种细胞功能的蛋白质参与了与巴甫洛夫条件作用相关的长期翻译后修饰。