Puighermanal Emma, Biever Anne, Valjent Emmanuel
CNRS, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
INSERM, U1191, Montpellier, France.
Bio Protoc. 2016 Feb 20;6(4):e1735. doi: 10.21769/BioProtoc.1735.
Activity-dependent local mRNA translation endows synapses to remodel their structure and function (Bramham and Wells, 2007). This process is tightly controlled by the state of phosphorylation of several components of the translational machinery including initiation factors and ribosomal proteins (Buffington et al., 2014). The present protocol describes a method to prepare striatal synaptoneurosomes, from adult mice, containing both pre- and postsynaptic elements in which the level of synaptic phospho-proteins can be quantified (Biever et al., 2015).
活性依赖的局部mRNA翻译使突触能够重塑其结构和功能(布拉姆哈姆和韦尔斯,2007年)。这一过程受到翻译机制中几个组分磷酸化状态的严格控制,这些组分包括起始因子和核糖体蛋白(布芬顿等人,2014年)。本实验方案描述了一种从成年小鼠制备纹状体突触神经小体的方法,该突触神经小体包含突触前和突触后元件,其中突触磷酸化蛋白的水平可以被定量(比弗等人,2015年)。