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真核生物细胞膜脂饱和度传感器

A Eukaryotic Sensor for Membrane Lipid Saturation.

机构信息

Department of Theoretical Biophysics, Max-Planck-Institute of Biophysics, 60438 Frankfurt, Germany.

Institute of Biochemistry and Buchmann and Institute for Molecular Life Sciences, Goethe University Frankfurt, I 60438 Frankfurt, Germany.

出版信息

Mol Cell. 2016 Jul 7;63(1):49-59. doi: 10.1016/j.molcel.2016.05.015. Epub 2016 Jun 16.

Abstract

Maintaining a fluid bilayer is essential for cell signaling and survival. Lipid saturation is a key factor determining lipid packing and membrane fluidity, and it must be tightly controlled to guarantee organelle function and identity. A dedicated eukaryotic mechanism of lipid saturation sensing, however, remains elusive. Here we show that Mga2, a transcription factor conserved among fungi, acts as a lipid-packing sensor in the ER membrane to control the production of unsaturated fatty acids. Systematic mutagenesis, molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a pivotal role of the oligomeric transmembrane helix (TMH) of Mga2 for intra-membrane sensing, and they show that the lipid environment controls the proteolytic activation of Mga2 by stabilizing alternative rotational orientations of the TMH region. This work establishes a eukaryotic strategy of lipid saturation sensing that differs significantly from the analogous bacterial mechanism relying on hydrophobic thickness.

摘要

维持流体双层对于细胞信号传递和存活至关重要。脂质饱和度是决定脂质堆积和膜流动性的关键因素,必须严格控制以保证细胞器的功能和身份。然而,专门的脂质饱和度感应的真核生物机制仍然难以捉摸。在这里,我们发现真菌中保守的转录因子 Mga2 作为内质网膜中的脂质堆积传感器,控制不饱和脂肪酸的产生。系统突变、分子动力学模拟和电子顺磁共振波谱学确定了 Mga2 的寡聚跨膜螺旋 (TMH) 在膜内感应中的关键作用,并表明脂质环境通过稳定 TMH 区域的替代旋转取向来控制 Mga2 的蛋白水解激活。这项工作建立了一种真核生物的脂质饱和度感应策略,与依赖疏水性厚度的类似细菌机制有显著差异。

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