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GDP 优先在异三聚体 G 蛋白的磷酸侧释放。

GDP release preferentially occurs on the phosphate side in heterotrimeric G-proteins.

机构信息

Institut des Biomolécules Max Mousseron-IBMM, CNRS UMR5247, Université Montpellier 1, Université Montpellier 2, Faculté de Pharmacie, Montpellier, France.

出版信息

PLoS Comput Biol. 2012;8(7):e1002595. doi: 10.1371/journal.pcbi.1002595. Epub 2012 Jul 19.

Abstract

After extra-cellular stimulation of G-Protein Coupled Receptors (GPCRs), GDP/GTP exchange appears as the key, rate limiting step of the intracellular activation cycle of heterotrimeric G-proteins. Despite the availability of a large number of X-ray structures, the mechanism of GDP release out of heterotrimeric G-proteins still remains unknown at the molecular level. Starting from the available X-ray structure, extensive unconstrained/constrained molecular dynamics simulations were performed on the complete membrane-anchored Gi heterotrimer complexed to GDP, for a total simulation time overcoming 500 ns. By combining Targeted Molecular Dynamics (TMD) and free energy profiles reconstruction by umbrella sampling, our data suggest that the release of GDP was much more favored on its phosphate side. Interestingly, upon the forced extraction of GDP on this side, the whole protein encountered large, collective motions in perfect agreement with those we described previously including a domain to domain motion between the two ras-like and helical sub-domains of G(α).

摘要

细胞外刺激 G 蛋白偶联受体 (GPCRs) 后,GDP/GTP 交换似乎是异三聚体 G 蛋白细胞内激活循环的关键限速步骤。尽管已经有大量的 X 射线结构,但异三聚体 G 蛋白中 GDP 释放的机制在分子水平上仍然未知。从现有的 X 射线结构出发,对与 GDP 结合的完整膜锚定 Gi 异三聚体复合物进行了广泛的无约束/约束分子动力学模拟,总模拟时间超过 500 纳秒。通过结合靶向分子动力学 (TMD) 和伞状采样重建自由能谱,我们的数据表明 GDP 的释放更有利于其磷酸侧。有趣的是,在对该侧进行强制提取 GDP 时,整个蛋白质会发生大的集体运动,与我们之前描述的完全一致,包括两个 Ras 样和螺旋亚域之间的域到域运动 G(α)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb2/3400569/4140a99c19fc/pcbi.1002595.g001.jpg

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