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Adsorption of charged protein residues on an inorganic nanosheet: Computer simulation of LDH interaction with ion channel

机译:无机纳米片上带电蛋白质残留的吸附:LDH与离子通道相互作用的计算机模拟

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摘要

Quasi-two-dimensional and hybrid nanomaterials based on layered double hydroxides (LDH), cationic clays, layered oxyhydroxides and hydroxides of metals possess large specific surface area and strong electrostatic properties with permanent or pH-dependent electric charge. Such nanomaterials may impact cellular electrostatics, changing the ion balance, pH and membrane potential. Selective ion adsorption/exchange may alter the transmembrane electrochemical gradient, disrupting potential-dependent cellular processes. Cellular proteins as a rule have charged residues which can be effectively adsorbed on the surface of layered hydroxide based nanomaterials. The aim of this study is to attempt to shed some light on the possibility and mechanisms of protein “adhesion” an LDH nanosheet and to propose a new direction in anticancer medicine, based on physical impact and strong electrostatics. An unbiased molecular dynamics simulation was performed and the combined process free energy estimation (COPFEE) approach was used.
机译:基于层状双氢氧化物(LDH),阳离子粘土,层状羟基氧化物和金属氢氧化物的准二维和杂化纳米材料具有大的比表面积和强的静电特性,具有永久性或pH依赖性电荷。此类纳米材料可能会影响细胞静电,从而改变离子平衡,pH和膜电位。选择性离子吸附/交换可能会改变跨膜电化学梯度,破坏电位依赖性细胞过程。通常,细胞蛋白质具有带电荷的残基,该残基可以有效地吸附在层状氢氧化物基纳米材料的表面上。这项研究的目的是试图阐明蛋白质“粘附” LDH纳米片的可能性和机理,并基于物理影响和强静电为抗癌医学提出新的方向。进行了无偏分子动力学模拟,并使用了组合过程自由能估计(COPFEE)方法。

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