对于同一个与DnaK和GroEL相伴结合的多的不同构造
S J Landry1, R Jordan, R McMacken
1Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas 75325-9041.
Nature
|January 30, 1992
概括
分子伴侣DnaK和GroEL以不同的方式结合. 使用NMR,这项研究揭示了采用扩展形状与DnaK和螺旋结构与GroEL,影响脊柱的移动性.
科学领域:
- 分子生物学分子生物学
- 结构生物学是结构生物学.
- 生物化学 生物化学
背景情况:
- DnaK (hsp70) 和GroEL (cpn60) 是大肠杆菌中必不可少的分子伴侣,代表保存的蛋白质家族.
- 分子伴侣在蛋白质折叠,稳定性和细胞功能中发挥着关键作用.
- 在分子层面上理解陪伴者-客户互动是解读细胞过程的关键.
研究的目的:
- 调查模型 (vsv-C) 结合两个不同的分子伴侣DnaK和GroEL时的构造状态.
- 阐明伴侣结合对骨和侧链流动性的影响.
主要方法:
- 在二维NMR光谱学中利用转移的核Overhauser效应 (tr-NOE).
- 分析了与DnaK和GroEL复合的vsv-C (KLIGVLSSLFRPK).
主要成果:
- 当与DnaK结合时,vsv-C采用了一个扩展的形状.
- 当与GroEL结合时,vsv-C采用螺旋形状.
- 与GroEL相比,与DnaK结合时,的骨干流动性显著降低.
- 当与GroEL比与DnaK结合时,侧链的移动性更受限制.
结论:
- DnaK和GroEL在结合中诱导出明显的形状变化.
- 伴侣诱导的形状偏好会以不同的方式影响片段的动态.
- 这些发现提供了关于分子陪伴者识别和处理基底蛋白的机制的见解.
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