生物化学分离和组装介导新生的链准和转位的膜组件
C V Nicchitta1, G Migliaccio, G Blobel
1Laboratory of Cell Biology, Howard Hughes Medical Institute, Rockefeller University, New York, New York 10021-6399.
Cell
|May 17, 1991
概括
研究人员隔离了信号识别粒子受体 (SRα),这对于新生的链准至关重要,将其与转位蛋白分开. 这将前体结合与转位分离,揭示了不同的序列反应组件.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 蛋白质生物化学 蛋白质生物化学
背景情况:
- 蛋白质向和转位是细胞中必不可少的过程.
- 信号识别粒子受体 (SRα) 在新生的链准中起作用.
- 了解涉及蛋白质转位的不同组件至关重要.
研究的目的:
- 生物化学分离和表征参与蛋白质转位的成分.
- 调查前体向和转位之间的关系.
- 为了确定前体结合和转位是否由不同的分子实体介导.
主要方法:
- 使用硫酸沉的微体洗剂提取物分化.
- 使用SRα丰富分数进行溶解试验.
- 补充蛋白质子分数添加和硫基导向色谱用于蛋白质耗尽.
主要成果:
- SRα从信号酶和其他微小蛋白质中分离出来.
- 重建的SRα分量支持前体向和延长停止释放,但缺乏转位活性.
- 通过添加单独的蛋白质分片,可以恢复转位活动,并且可以在保持向的同时耗尽转位组件.
结论:
- 前体结合和转位是不同的连续反应.
- 蛋白质向和转位是由单独的组件介导的.
- 信号识别粒子受体 (SRα) 主要参与准,而不是转移.
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