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How a protein can remain stable in a solvent with high content of urea: insights from molecular dynamics simulation of Candida antarctica lipase B in urea: choline chloride deep eutectic solvent

机译:如何在尿素含量高含量的溶剂中含有蛋白质:来自尿素中的念珠菌抗野胶脂肪酶B的分子动力学模拟的见解:氯化胆碱深度共晶溶剂

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Deep eutectic solvents (DESs) are utilized as green and inexpensive alternatives to classical ionic liquids. It has been known that some of DESs can be used as solvent in the enzymatic reactions to obtain very green chemical processes. DESs are quite poorly understood at the molecular level. Moreover, we do not know much about the enzyme microstructure in such systems. For example, how some hydrolase can remain active and stable in a deep eutectic solvent including 9 M of urea? In this study, the molecular dynamics of DESs as a liquid was simulated at the molecular level. Urea: choline chloride as a well-known eutectic mixture was chosen as a model DES. The behavior of the lipase as a biocatalyst was studied in this system. For comparison, the enzyme structure was also simulated in 8M urea. The thermal stability of the enzyme was also evaluated in DESs, water, and 8M urea. The enzyme showed very good conformational stability in the urea: choline chloride mixture with about 66% urea (9 M) even at high temperatures. The results are in good agreement with recent experimental observations. In contrast, complete enzyme denaturation occurred in 8M urea with only 12% urea in water. It was found that urea molecules denature the enzyme by interrupting the intra-chain hydrogen bonds in a "direct denaturation mechanism". However, in a urea:choline chloride deep eutectic solvent, as a result of hydrogen bonding with choline and chloride ions, urea molecules have a low diffusion coefficient and cannot reach the protein domains. Interestingly, urea, choline, and chloride ions form hydrogen bonds with the surface residues of the enzyme which, instead of lipase denaturation, leads to greater enzyme stability. To the best of our knowledge, this is the first study in which the microstructural properties of a macromolecule are examined in a deep eutectic solvent.
机译:深度共晶溶剂(DESS)用作典型离子液体的绿色和廉价的替代品。已知一些Dess可以用作酶促反应中的溶剂,以获得非常绿色的化学过程。 Dess在分子水平上很糟糕地理解。此外,我们对这种系统中的酶微结构不太了解。例如,一些水解酶可以在包含9米尿素的深层共晶溶剂中保持活性和稳定性?在该研究中,在分子水平下模拟了作为液体的DES的分子动力学。尿素:选择氯化胆碱作为众所周知的共晶混合物作为模型DES。在该系统中研究了脂肪酶作为生物催化剂的行为。为了比较,酶结构也在8M尿素中模拟。还在Dess,Water和8M尿素中评估酶的热稳定性。酶在尿素中表现出非常好的构象稳定性:即使在高温下,氯化胆碱混合物含量约为66%尿素(9μm)。结果与最近的实验观察结果良好。相比之下,在8M尿素中发生完整的酶变性,仅在水中只有12%的尿素。发现尿素分子通过中断在“直接变性机制”中的链内氢键来满足酶。然而,在尿素中:氯化胆碱深对共晶溶剂,由于与胆碱和氯离子的氢键,尿素分子具有低扩散系数并且不能到达蛋白质结构域。有趣的是,尿素,胆碱和氯离子与酶的表面残留物形成氢键,而不是脂肪酶变性,导致更大的酶稳定性。据我们所知,这是第一研究,其中在深度共晶溶剂中检查大分子的微观结构性质。

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