首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Formation versus Hydrolysis of the Peptide Bond from a Quantum-mechanical Viewpoint: The Role of Mineral Surfaces and Implications for the Origin of Life
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Formation versus Hydrolysis of the Peptide Bond from a Quantum-mechanical Viewpoint: The Role of Mineral Surfaces and Implications for the Origin of Life

机译:从量子力学观点看肽键的形成与水解:矿物质表面的作用及其对生命起源的影响

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摘要

The condensation (polymerization by water elimination) of molecular building blocks to yield the first active biopolymers (e.g. of amino acids to form peptides) during primitive Earth is an intriguing question that nowadays still remains open since these processes are thermodynamically disfavoured in highly dilute water solutions. In the present contribution, formation and hydrolysis of glycine oligopeptides occurring on a cluster model of sanidine feldspar (001) surface have been simulated by quantum mechanical methods. Results indicate that the catalytic interplay between Lewis and Brønsted sites both present at the sanidine surface, in cooperation with the London forces acting between the biomolecules and the inorganic surface, plays a crucial role to: i) favour the condensation of glycine to yield oligopeptides as reaction products; ii) inhibit the hydrolysis of the newly formed oligopeptides. Both facts suggest that mineral surfaces may have helped in catalyzing, stabilizing and protecting from hydration the oligopeptides formed in the prebiotic era.
机译:在原始地球期间,分子构件的缩合(通过除水聚合)以生成第一种活性生物聚合物(例如,氨基酸形成肽)是一个引人入胜的问题,由于这些过程在高度稀释的水溶液中在热力学上不利,因此今天仍然开放。在目前的贡献中,已经通过量子力学方法模拟了在山idine长石(001)表面的簇模型上发生的甘氨酸寡肽的形成和水解。结果表明,均存在于Sanidine表面的Lewis位点和Brønsted位点之间的催化相互作用,与作用于生物分子和无机表面之间的伦敦力合作,起着至关重要的作用:i)促进甘氨酸的缩合生成寡肽,如反应产物; ii)抑制新形成的寡肽的水解。这两个事实都表明,矿物质表面可能有助于催化,稳定和防止水合形成益生元时代形成的寡肽。

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