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真核生物乳酸脱氢酶中“变构样”大规模运动的热激活。

Thermal activation of 'allosteric-like' large-scale motions in a eukaryotic Lactate Dehydrogenase.

机构信息

Laboratoire de Biochimie Théorique, IBPC, CNRS UPR9080, Univ. Paris Diderot, Sorbonne Paris Cité, 13 rue Pierre et Marie Curie, 75005, Paris, France.

Univ. Grenoble Alpes - Laboratoire TIMC/IMAG UMR CNRS 5525, Grenoble Pavillon Taillefer Domaine de la merci, 38700 La Tronche, France.

出版信息

Sci Rep. 2017 Jan 23;7:41092. doi: 10.1038/srep41092.

Abstract

Conformational changes occurring during the enzymatic turnover are essential for the regulation of protein functionality. Individuating the protein regions involved in these changes and the associated mechanical modes is still a challenge at both experimental and theoretical levels. We present here a detailed investigation of the thermal activation of the functional modes and conformational changes in a eukaryotic Lactate Dehydrogenase enzyme (LDH). Neutron Spin Echo spectroscopy and Molecular Dynamics simulations were used to uncover the characteristic length- and timescales of the LDH nanoscale motions in the apo state. The modes involving the catalytic loop and the mobile region around the binding site are activated at room temperature, and match the allosteric reorganisation of bacterial LDHs. In a temperature window of about 15 degrees, these modes render the protein flexible enough and capable of reorganising the active site toward reactive configurations. On the other hand an excess of thermal excitation leads to the distortion of the protein matrix with a possible anti-catalytic effect. Thus, the temperature activates eukaryotic LDHs via the same conformational changes observed in the allosteric bacterial LDHs. Our investigation provides an extended molecular picture of eukaryotic LDH's conformational landscape that enriches the static view based on crystallographic studies alone.

摘要

在酶促转化过程中发生的构象变化对于蛋白质功能的调节至关重要。在实验和理论水平上,确定参与这些变化的蛋白质区域和相关的力学模式仍然是一个挑战。在这里,我们详细研究了真核乳酸脱氢酶(LDH)的功能模式和构象变化的热激活。利用中子旋转回波光谱和分子动力学模拟揭示了apo 状态下 LDH 纳米运动的特征长度和时间尺度。涉及催化环和结合位点周围可移动区域的模式在室温下被激活,与细菌 LDH 的变构重组相匹配。在大约 15 度的温度范围内,这些模式使蛋白质足够灵活,并能够将活性位点重新组织成反应性构型。另一方面,过多的热激发会导致蛋白质基质的变形,可能产生反催化作用。因此,温度通过在变构细菌 LDH 中观察到的相同构象变化激活真核 LDH。我们的研究提供了真核 LDH 构象景观的扩展分子图像,丰富了仅基于晶体学研究的静态视图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0738/5253740/93f26e20a21c/srep41092-f1.jpg

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