Literature DB >> 8298454

Thermodynamics of unfolding for turkey ovomucoid third domain: thermal and chemical denaturation.

L Swint1, A D Robertson.   

Abstract

We have used thermal and chemical denaturation to characterize the thermodynamics of unfolding for turkey ovomucoid third domain (OMTKY3). Thermal denaturation was monitored spectroscopically at a number of wave-lengths and data were subjected to van't Hoff analysis; at pH 2.0, the midpoint of denaturation (Tm) occurs at 58.6 +/- 0.4 degrees C and the enthalpy of unfolding at this temperature (delta Hm) is 40.8 +/- 0.3 kcal/mol. When Tm was perturbed by varying pH and denaturant concentration, the resulting plots of delta Hm versus Tm yield a mean value of 590 +/- 120 cal/(mol.K) for the change in heat capacity upon unfolding (delta Cp). A global fit of the same data to an equation that includes the temperature dependence for the enthalpy of unfolding yielded a value of 640 +/- 110 cal/(mol.K). We also performed a variation of the linear extrapolation method described by Pace and Laurents, which is an independent method for determining delta Cp (Pace, C.N. & Laurents, D., 1989, Biochemistry 28, 2520-2525). First, OMTKY3 was thermally denatured in the presence of a variety of denaturant concentrations. Linear extrapolations were then made from isothermal slices through the transition region of the denaturation curves. When extrapolated free energies of unfolding (delta Gu) were plotted versus temperature, the resulting curve appeared linear; therefore, delta Cp could not be determined. However, the data for delta Gu versus denaturant concentration are linear over an extraordinarily wide range of concentrations. Moreover, extrapolated values of delta Gu in urea are identical to values measured directly.

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Year:  1993        PMID: 8298454      PMCID: PMC2142319          DOI: 10.1002/pro.5560021205

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  41 in total

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Journal:  Biochim Biophys Acta       Date:  1959-12

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Journal:  Anal Biochem       Date:  1974-05       Impact factor: 3.365

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Journal:  Methods Enzymol       Date:  1973       Impact factor: 1.600

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Authors:  C N Pace; K E Vanderburg
Journal:  Biochemistry       Date:  1979-01-23       Impact factor: 3.162

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Authors:  P L Privalov
Journal:  Adv Protein Chem       Date:  1979

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Journal:  Biochim Biophys Acta       Date:  1981-02-27

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Journal:  Biophys Chem       Date:  1976-01       Impact factor: 2.352

10.  Helix-coil transition of polyl-glutamic acid and polyl-lysine in D2O.

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Journal:  Biochemistry       Date:  1965-07       Impact factor: 3.162

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  37 in total

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Journal:  Protein Sci       Date:  2003-04       Impact factor: 6.725

10.  Corynebacterium diphtheriae HmuT: dissecting the roles of conserved residues in heme pocket stabilization.

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