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- W1986876479 abstract "The factors that determine the stability of antiparallel β-sheets are consideredviaa theoretical analysis of conformational free energies. A series of idealized model polyalanine β-sheets are built with constraints such that the angular geometry of hydrogen bonding varies in the range observed in proteins while hydrogen bonding distance remains fixed. The conformations of the sheets generated in this way have a broad distribution of twist angles ranging from highly twisted left-handed to highly twisted right-handed orientations. The association free energies of the sheets are calculated with a gas phase CHARMM potential and FDPB/γ solvation models. Left-handed structures are found to be less stable than right handed structures due to intrachain steric hindrance in isolated left-handed strands. This explains why antiparallel β-sheets in proteins are invariably twisted in the right-handed direction. The free energy surface for right-handed sheets shows particular preference for conformations ranging from flat to those that exhibit a pronounced right-handed twist. This suggests that antiparallel β-sheets can adopt a variety of right-handed conformations, a result that is consistent with observations on known proteins. In parallel with our study of α-helices we find that van der Waals and hydrophobic interactions are the primary factor stabilizing polyalanine β-sheets, while electrostatic interactions including hydrogen bonding are found to be destabilizing. However, in contrast to helices, the net change in conformational free energy involving only backbone-backbone interactions (including β-carbons) is not sufficient to overcome the loss in configurational entropy that accompanies sheet formation. Rather we suggest that cross-strand non-polar side-chain–side-chain interactions are essential for sheet formation, explaining why large non-polar amino acids have the greatest sheet forming propensities. Thus, sheet propensities involve pairwise interactions and are expected to be context dependent, as has been observed in recent experiments." @default.
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- W1986876479 date "1995-09-01" @default.
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- W1986876479 title "Free Energy Determinants of Secondary Structure Formation: II. Antiparallel β-Sheets" @default.
- W1986876479 doi "https://doi.org/10.1006/jmbi.1995.0503" @default.
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