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Article Dans Une Revue Soft Matter Année : 2011

Stability of the gramicidin-A channel structure in view of nanofiltration: a computational and experimental study

Résumé

The secondary, ternary and quaternary structures of the biological ion channel Gramicidin-A are investigated by means of UV-visible and fluorescence spectroscopies, and by computational simulations in water/methanol solvent with various molar ratios. Both experiments and molecular dynamics calculations show that the two considered conformations, i.e. the head-to-head and double-stranded β-helix dimers, behave differently with regard to their stability as a function of the methanol content in the water/methanol mixture. To sum-up, calculations show that the double-stranded dimer is stabilized by methanol, even at low content, while the head-to-head dimer conformation breaks into two monomers which remain however coupled whatever the water/methanol mixture. In pure water and low methanol content, the resulting single β-helix structure is maintained due to the stabilization of the channel by water molecules and cations.

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Chimie
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Dates et versions

hal-00733694 , version 1 (19-09-2012)

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D. Bonhenry, S. Kraszewski, S. Picaud, Christophe Ramseyer, Sebastien Balme, et al.. Stability of the gramicidin-A channel structure in view of nanofiltration: a computational and experimental study. Soft Matter, 2011, 7 (22), pp.10651-10659. ⟨10.1039/c1sm06277h⟩. ⟨hal-00733694⟩
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