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首页> 外文期刊>Nanoscale >Surface-assisted assembly of a histidine-rich lipidated peptide for simultaneous exfoliation of graphite and functionalization of graphene nanosheets
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Surface-assisted assembly of a histidine-rich lipidated peptide for simultaneous exfoliation of graphite and functionalization of graphene nanosheets

机译:Surface-assisted装配问题lipidated肽同时剥落石墨和石墨烯的功能化nanosheets

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Biological molecules have promising potential to exfoliate graphite and produce biocompatible graphene nano-materials for biomedical applications. Here, a systematic design of a histidine-rich lipidated peptide sequence is presented that simultaneously exfoliates graphite flakes and functionalizes the resulting graphene nanosheets (approximate to 150 nm lateral size) with long-term dispersion stability in aqueous solution (8 months). The details of peptide/peptide and peptide/graphite interactions are probed using various microscopy, spectroscopy and molecular dynamics simulation methods. The results show that histidine and stearic acid interact with the graphite surface through - stacking and hydrophobic forces, respectively. Surface-assisted assembly of peptide molecules is then initiated via hydrogen bonds between deprotonated histidine segments, and a textured peptide nano-structure is formed. The work of adhesion between the peptide and graphite is found to be high enough to promote exfoliation of graphite flakes through layer-by-layer peeling of graphene nanosheets. The positively charged arginine in the peptide is exposed outward, and is responsible for the stable dispersion. The peptide molecules are sufficiently small, presenting the possibility to insert into and increase the spacing between the graphitic layers for enhanced exfoliation. The peptide-functionalized graphene nanosheets not only show great biocompatibility with cells in vitro, but also enhance cancer drug uptake by the cells.
机译:生物分子有前途的潜力片状剥落石墨和生产生物相容性石墨烯纳米材料的生物医学应用程序。富含组氨酸lipidated肽序列提出同时中的石墨片,使职能化产生的石墨烯nanosheets(大约150海里横向大小)与长期在水分散稳定性解决方案(在8个月)。肽/多肽和肽/石墨相互作用使用各种显微镜探测,光谱和分子动力学模拟方法。结果表明,组氨酸和硬脂酸与石墨表面通过——交互分别叠加和疏水的力量。Surface-assisted肽分子的组装然后通过氢键之间发起的deprotonated组氨酸段,和变形肽纳米结构形成。肽与石墨之间的附着力高到足以促进表皮脱落通过逐层剥离的石墨薄片石墨烯nanosheets。精氨酸肽中向外暴露负责稳定分散。肽分子足够小,的插入和可能性增加石墨层之间的间距增强表皮脱落。peptide-functionalized石墨烯nanosheets不只显示伟大的生物相容性和细胞体外,还提高抗癌药物的吸收细胞。

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