Ureaerature phase diagrams capture the thermodynamics of denatured state expansion that accompany protein unfolding

Alexander Tischer, Matthew T Auton

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

We have analyzed the thermodynamic properties of the von Willebrand factor (VWF) A3 domain using urea-induced unfolding at variable temperature and thermal unfolding at variable urea concentrations to generate a phase diagram that quantitatively describes the equilibrium between native and denatured states. From this analysis, we were able to determine consistent thermodynamic parameters with various spectroscopic and calorimetric methods that define the urea-temperature parameter plane from cold denaturation to heat denaturation. Urea and thermal denaturation are experimentally reversible and independent of the thermal scan rate indicating that all transitions are at equilibrium and the van't Hoff and calorimetric enthalpies obtained from analysis of individual thermal transitions are equivalent demonstrating two-state character. Global analysis of the urea-temperature phase diagram results in a significantly higher enthalpy of unfolding than obtained from analysis of individual thermal transitions and significant cross correlations describing the urea dependence of δH0 and δC0 P that define a complex temperature dependence of the m-value. Circular dichroism (CD) spectroscopy illustrates a large increase in secondary structure content of the urea-denatured state as temperature increases and a loss of secondary structure in the thermally denatured state upon addition of urea. These structural changes in the denatured ensemble make up ~40% of the total ellipticity change indicating a highly compact thermally denatured state. The difference between the thermodynamic parameters obtained from phase diagram analysis and those obtained from analysis of individual thermal transitions illustrates that phase diagrams capture both contributions to unfolding and denatured state expansion and by comparison are able to decipher these contributions.

Original languageEnglish (US)
Pages (from-to)1147-1160
Number of pages14
JournalProtein Science
Volume22
Issue number9
DOIs
StatePublished - Sep 2013

Fingerprint

Protein Unfolding
Thermodynamics
Phase diagrams
Urea
Hot Temperature
Denaturation
Proteins
Temperature
Enthalpy
Circular dichroism spectroscopy
Phase Transition
von Willebrand Factor
Circular Dichroism
Spectrum Analysis
Thermodynamic properties

Keywords

  • Circular dichroism
  • Denatured state expansion
  • Differential scanning calorimetry
  • Fluorescence
  • Urea-temperature phase diagram
  • Von Willebrand factor

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Medicine(all)

Cite this

Ureaerature phase diagrams capture the thermodynamics of denatured state expansion that accompany protein unfolding. / Tischer, Alexander; Auton, Matthew T.

In: Protein Science, Vol. 22, No. 9, 09.2013, p. 1147-1160.

Research output: Contribution to journalArticle

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