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2000
Volume 12, Issue 3
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

Basic concepts about two-state, cooperative protein folding and its relation to first-order phase transitions are reviewed. Minimalist models capable of reproducing the required free energy barrier between folded and unfolded macroscopic states are described. A significantly more restrictive “calorimetric” criterion is also discussed, which is based on direct comparison between model and experimental heat capacities with additional assumptions about conformational enthalpy variation in the unfolded state.

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/content/journals/ppl/10.2174/0929866053587101
2005-04-01
2025-05-25
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