About: Force-Field Dependence of Chignolin Folding and Misfolding: Comparison with Experiment and Redesign     Goto   Sponge   NotDistinct   Permalink

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  • We study the folding of the designed hairpin chignolin, using simulations with four different force fields. Interestingly, we find a misfolded, out-of-register, structure comprising 20-50% of the ordered structures with three force fields, but not with a fourth. A defining feature of the misfold is that Gly-7 adopts a beta(PR) conformation rather than alpha(L). By reweighting, we show that differences between the force fields can mostly be attributed to differences in glycine properties. Benchmarking against NMR data suggests that the preference for beta(PR) is not a force-field artifact. For chignolin, we show that including the misfold in the ensemble results in back-recalculated NMR observables in slightly better agreement with experiment than parameters calculated from a folded ensemble only. For comparison, we show by NMR and circular dichroism spectroscopy that the G7K mutant of chignolin, in which formation of this misfold is impossible, is well folded with stability similar to the wild-type and does not populate the misfolded state in simulation. Our results highlight the complexity of interpreting NMR data for small, weakly structured, peptides in solution, as well as the importance of accurate glycine parameters in force fields, for a correct description of turn structures.
  • We study the folding of the designed hairpin chignolin, using simulations with four different force fields. Interestingly, we find a misfolded, out-of-register, structure comprising 20-50% of the ordered structures with three force fields, but not with a fourth. A defining feature of the misfold is that Gly-7 adopts a beta(PR) conformation rather than alpha(L). By reweighting, we show that differences between the force fields can mostly be attributed to differences in glycine properties. Benchmarking against NMR data suggests that the preference for beta(PR) is not a force-field artifact. For chignolin, we show that including the misfold in the ensemble results in back-recalculated NMR observables in slightly better agreement with experiment than parameters calculated from a folded ensemble only. For comparison, we show by NMR and circular dichroism spectroscopy that the G7K mutant of chignolin, in which formation of this misfold is impossible, is well folded with stability similar to the wild-type and does not populate the misfolded state in simulation. Our results highlight the complexity of interpreting NMR data for small, weakly structured, peptides in solution, as well as the importance of accurate glycine parameters in force fields, for a correct description of turn structures. (en)
Title
  • Force-Field Dependence of Chignolin Folding and Misfolding: Comparison with Experiment and Redesign
  • Force-Field Dependence of Chignolin Folding and Misfolding: Comparison with Experiment and Redesign (en)
skos:prefLabel
  • Force-Field Dependence of Chignolin Folding and Misfolding: Comparison with Experiment and Redesign
  • Force-Field Dependence of Chignolin Folding and Misfolding: Comparison with Experiment and Redesign (en)
skos:notation
  • RIV/61989592:15310/12:33142576!RIV13-MSM-15310___
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  • P(ED2.1.00/03.0058), P(EE2.3.20.0017), P(GD203/09/H046), S
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  • 8
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  • 136927
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  • RIV/61989592:15310/12:33142576
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  • parameters; miniprotein; polypeptides; peptides; explicit water; unfolded state; protein backbone; beta-hairpin; helix-coil transition; molecular-dynamics simulations (en)
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  • US - Spojené státy americké
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  • [D0E89A260C49]
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  • Biophysical Journal
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  • 102
http://linked.open...iv/tvurceVysledku
  • Otyepka, Michal
  • Best, Robert
  • De Simone, Alfonso
  • Kührová, Petra
http://linked.open...ain/vavai/riv/wos
  • 000303003300024
issn
  • 0006-3495
number of pages
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  • 10.1016/j.bpj.2012.03.024
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  • 15310
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