Surface-assisted assembly of a histidine-rich lipidated peptide for simultaneous exfoliation of graphite and functionalization of graphene nanosheets

被引:43
|
作者
Zhang, Lei [1 ,2 ,3 ]
Sheng, Yuebiao [4 ,5 ]
Yazdi, Alireza Zehtab [1 ,2 ]
Sarikhani, Kaveh [1 ,2 ]
Wang, Feng [2 ,6 ]
Jiang, Yunsheng [1 ]
Liu, Juewen [2 ,6 ]
Zheng, Tao [3 ]
Wang, Wei [4 ]
Ouyang, Pingkai [3 ]
Chen, Pu [1 ,2 ,3 ]
机构
[1] Univ Waterloo, Dept Chem Engn, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
[2] Univ Waterloo, Waterloo Inst Nanotechnol, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
[3] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China
[4] Nanjing Univ, Dept Phys, Nanjing 210093, Jiangsu, Peoples R China
[5] Nanjing Univ, High Performance Comp Ctr, Nanjing 210093, Jiangsu, Peoples R China
[6] Univ Waterloo, Dept Chem, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CARBON NANOTUBES; SMALL-MOLECULE; DELIVERY; GROWTH; NANOPARTICLES; NANOMATERIALS; MECHANISM; PROTEINS; SIRNA;
D O I
10.1039/c8nr08397e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:2999 / 3012
页数:14
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