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Two-state folding over a weak free-energy barrier

Författare

Summary, in English

We present a Monte Carlo study of a model protein with 54 amino acids that folds directly to its native three-helix-bundle state without forming any well-defined intermediate state. The free-energy barrier separating the native and unfolded states of this protein is found to be weak, even at the folding temperature. Nevertheless, we find that melting curves to a good approximation can be described in terms of a simple two-state system, and that the relaxation behavior is close to single exponential. The motion along individual reaction coordinates is roughly diffusive on timescales beyond the reconfiguration time for a single helix. A simple estimate based on diffusion in a square-well potential predicts the relaxation time within a factor of two.

Publiceringsår

2003

Språk

Engelska

Sidor

1457-1465

Publikation/Tidskrift/Serie

Biophysical Journal

Volym

85

Issue

3

Dokumenttyp

Artikel i tidskrift

Förlag

Cell Press

Ämne

  • Biophysics

Status

Published

ISBN/ISSN/Övrigt

  • ISSN: 1542-0086