Nano-confinement of biomolecules: Hydrophilic confinement promotes structural order and enhances mobility of water molecules
Molecular dynamics simulations have been used to investigate the confinement packing characteristics of small hydrophilic (N-acetyl-glycine-methylamide, Nagma) and hydrophobic (N-acetyl-leucine-methylamide, Nalma) biomolecules in large diameter single-wall carbon nanotubes (SWCNTs). We find that hydrophilic biomolecules easily fill the nanotube and self organize into a geometrical configuration which reminds the water structural organization under SWCNT confinement. The packing of hydrophilic biomolecules inside the cylinder confines all water molecules in its core, which enhances their mobility. Conversely, hydrophobic biomolecules accommodate into the nanotubes with a trend for homogeneous filling, which generate unstable small pockets of water and drive toward a state of dehydration. These results shed light on key parameters important for the encapsulation of biomolecules with direct relevance for long-term storage and prevention of degradation.
Keywordsnano-confinement protein folding hydration water carbon nanotube drug delivery
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- Cass, T.; Ligler, F. S. Immobilized Biomolecules in Analysis: A Practical Approach; Oxford University Press: Oxford, 1998.Google Scholar
- Pantarotto, D.; Briand, J. P.; Prato, M.; Bianco, A. Translocation of bioactive peptides across cell membranes by carbon nanotubes. Chem. Commun. 2004, 16–17.Google Scholar
- Paineau, E.; Albouy, P. A.; Rouzière, S.; Orecchini, A.; Rols, S.; Launois, P. X-ray scattering determination of the structure of water during carbon nanotube filling. Nano Lett. 2013, 13, 1751–1756.Google Scholar
- MacKerell, A. D. Jr.; Feig, M.; Brooks, C. L. 3rd. Extending the treatment of backbone energetics in protein force fields: Limitations of gas-phase quantum mechanics in reproducing protein conformational distributions in molecular dynamics simulations. J. Comput. Chem. 2004, 25, 1400–1415.CrossRefGoogle Scholar