Conformational Changes of the Protein Domains Upon Binding with Carbon Nanotubes Studied by Molecular Dynamics Simulations

Title: Conformational Changes of the Protein Domains Upon Binding with Carbon Nanotubes Studied by Molecular Dynamics Simulations

Volume: 2 Issue: 1

Author(s): Guanghong Zuo, Peng Xiu, Xin Zhou, Ruhong Zhou and Haiping Fang

Affiliation:

Keywords: Protein, Carbon nanotube, Molecular dynamics and Conformational change, coarse-grained, protein streptavidins, Saccharomyces cerevisiae., C-terminus, aromatic residue, spectroscopy, hydrophobic surface

Abstract: The interactions between the nanoscale particles, such as the carbon nanotubes, and biomolecules are essential to the nanoscale particle based biotechnology and biomedical applications, such as gene delivery, cellular imaging, tumor therapy. However, how the structure changes and whether the functions of the biomolecules are affected due to the existence of nanoscale particles are still poorly understood. In this paper, we review some of our recent progresses, which are based on the large scale molecular dynamics simulations, towards this direction. In our studies, by using an all-α domain named HP35 and an all-β domain named YJQ8WW as the examples, we show that the single-walled carbon nanotube (SWCNT), a typical form of hydrophobic nanoscale particle, can considerably change both the secondary and the tertiary structures of the proteins and form the protein-SWCNT complexes, in which the unfolded part of the proteins wrap around the SWCNT. The hydrophobic interaction and π-π stacking interaction between the nanoscale particles and the hydrophobic residues are found to play important roles in our observation.

Cite this article as:

Zuo Guanghong, Xiu Peng, Zhou Xin, Zhou Ruhong and Fang Haiping, Conformational Changes of the Protein Domains Upon Binding with Carbon Nanotubes Studied by Molecular Dynamics Simulations, Current Physical Chemistry 2012; 2 (1) . https://dx.doi.org/10.2174/1877946811202010012