An investigation into non-covalent functionalization of a single-walled carbon nanotube and a graphene sheet with protein G:A combined experimental and molecular dynamics study

被引:19
作者
Ebrahim-Habibi, Mohammad-Bagher [1 ]
Ghobeh, Maryam [2 ]
Mahyari, Farzaneh Aghakhani [3 ]
Rafii-Tabar, Hashem [1 ]
Sasanpour, Pezhman [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Phys & Biomed Engn, Tehran, Iran
[2] Islamic Azad Univ, Sci & Res Branch, Dept Biol, Tehran, Iran
[3] Sharif Univ Technol, Dept Phys, Tehran, Iran
关键词
ELECTROCHEMICAL IMMUNOSENSOR; LABEL-FREE; NANOPARTICLES; ADSORPTION; PEPTIDES; IMMOBILIZATION; IMMUNOASSAY; DISPERSIONS; ORIENTATION; BIOSENSOR;
D O I
10.1038/s41598-018-37311-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Investigation of non-covalent interaction of hydrophobic surfaces with the protein G (PrG) is necessary due to their frequent utilization in immunosensors and ELISA. It has been confirmed that surfaces, including carbonous-nanostructures (CNS) could orient proteins for a better activation. Herein, PrG interaction with single-walled carbon nanotube (SWCNT) and graphene (Gra) nanostructures was studied by employing experimental and MD simulation techniques. It is confirmed that the PrG could adequately interact with both SWCNT and Gra and therefore fine dispersion for them was achieved in the media. Results indicated that even though SWCNT was loaded with more content of PrG in comparison with the Gra, the adsorption of the PrG on Gra did not induce significant changes in the IgG tendency. Several orientations of the P rG were adopted in the presence of SWCNT or Gra; however, SWCNT could block the PrG-FcR. Moreover, it was confirmed that SWCNT reduced the alpha-helical structure content in the PrG. Reduction of alpha-helical structure of the PrG and improper orientation of the PrG-SWCNT could remarkably decrease the PrG tendency to the Fc of the IgG. Importantly, the Gra could appropriately orient the PrG by both exposing the PrG-FcR and also by blocking the fragment of the PrG that had tendency to interact with Fab in IgG.
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页数:18
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