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一种活性脂质结合的寡糖变酶的结构和机制
Camilo Perez1, Sabina Gerber1, Jérémy Boilevin2
1Institute of Molecular Biology and Biophysics, ETH Zürich, CH-8093 Zürich, Switzerland.
Nature
|August 13, 2015
概括
该ABC输送器PglK转换脂结寡糖为N结蛋白糖化. 它的机制涉及向外的状态,头部进入腔,而尾部仍然暴露在膜上.
科学领域:
- 生物化学
- 分子生物学
- 结构生物学
背景情况:
- 膜脂翻转对于细胞过程至关重要,但在能量方面不利.
- 酶催化了这个过程,但它们的机制在很大程度上是未知的.
- 脂质结合的寡糖是N结合蛋白质糖化中的必不可少的供体.
研究的目的:
- 为了阐明PglK的机制,一个ABC输送器催化了Campylobacter jejuni中的脂质结合的寡糖转换.
- 了解PglK如何促进这些复杂分子的转移.
主要方法:
- 在不同的形状状态下PglK的晶体结构.
- 一个新开发的体外翻转试验.
- 在Campylobacter jejuni的体内研究.
主要成果:
- PglK表现出向内和向外的形状,向外的状态对于翻转至关重要.
- 酸-寡糖体头组进入转位腔,与充电残留物相互作用.
- 脂质尾部结合并激活PglK,但在整个反应过程中仍然暴露在脂质双层中.
结论:
- PglK介导的翻转机制与正规的交替访问模式不同.
- 这项研究为ABC输送器的脂结寡糖转换提供了结构和机制基础.
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