Blau S E, Smith T M, Stone G C
Department of Neurobiology, Nathan Kline Institute, Orangeburg, NY 10962.
Neurochem Res. 1992 Aug;17(8):809-15. doi: 10.1007/BF00969017.
A procedure for labeling rat CNS proteins in vivo which is useful for behavioral and pharmacological studies has been developed. Intraventricular administration of 35S-methionine through bilateral indwelling cannulae provided reproducible and highly specific radiolabeling of proteins from frontal cortex (FC), parietal cortex (PC), occipital cortex (OC), striatum (ST), septal nuclei (SN), amygdala (AM), hippocampus (HIP), thalamus (TH), brain stem (BS) and cerebellum (CB). Relative rates of synthesis of over 200 individual proteins were subsequently analyzed by 2DGE. Regional analysis demonstrated increased labeling of a protein of MW 28 kD and pI 6.4 in the hippocampus that was barely detectable in striatum of control rats. In heat-shocked animals, there was increased relative synthesis of the 74 kD Heat Shock Protein in both the septal nuclei and hippocampus.
已开发出一种用于体内标记大鼠中枢神经系统蛋白质的方法,该方法对行为学和药理学研究很有用。通过双侧留置套管脑室内注射35S-甲硫氨酸可对额叶皮质(FC)、顶叶皮质(PC)、枕叶皮质(OC)、纹状体(ST)、隔核(SN)、杏仁核(AM)、海马体(HIP)、丘脑(TH)、脑干(BS)和小脑(CB)的蛋白质进行可重复且高度特异性的放射性标记。随后通过二维凝胶电泳(2DGE)分析了200多种单个蛋白质的相对合成速率。区域分析表明,在海马体中一种分子量为28 kD、等电点为6.4的蛋白质标记增加,而在对照大鼠的纹状体中几乎检测不到。在热休克动物中,隔核和海马体中74 kD热休克蛋白的相对合成均增加。