Literature DB >> 11286558

Volume, expansivity and isothermal compressibility changes associated with temperature and pressure unfolding of Staphylococcal nuclease.

H Seemann1, R Winter, C A Royer.   

Abstract

We have characterized the temperature- and pressure-induced unfolding of staphylococcal nuclease (Snase) using high precision densitometric measurements. The changes in the apparent specific volume, expansion coefficient and isothermal compressibility were determined by these measurements. To our knowledge, these are the first measurements of the volume and isothermal compressibility changes of a protein undergoing pressure-induced unfolding. In order to aid in interpreting the temperature and pressure dependence of the apparent specific volume of Snase, we have also carried out differential scanning calorimetry under the solution conditions which are used for the volumetric studies. We have seen that large compensating volume and compressibility effects accompany the temperature and pressure-induced protein unfolding. Measurements of the apparent specific volume and thermal expansion coefficient of Snase at ambient pressure indicate the formation of a pre-transitional, molten globule type of intermediate structure about 10 degrees C below the actual unfolding temperature of the protein. Compared to the folded state, the apparent specific volume of the unfolded protein is about 0.3-0.5 % smaller. In addition, we investigated the pressure dependence of the apparent specific volume of Snase at a number of different temperatures. At 45 degrees C we calculate a decrease in apparent specific volume due to pressure-induced unfolding of -3.3 10(-3) cm(3) g(-1) or -55 cm(3) mol(-1). The threefold increase in compressibility between 40 and 70 MPa reflects a transition to a partially unfolded state, which is consistent with our results obtained for the radius of gyration of the pressure-denatured state of Snase. At the lower temperature of 35 degrees C, a significant increase in compressibility around 30 MPa is indicative of the formation of a pressure-induced molten globule-like intermediate. Changes in the apparent volume, expansion coefficient and isothermal compressibility are discussed in terms of instrinsic, hydrational and thermal contributions accompanying the unfolding transition. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11286558     DOI: 10.1006/jmbi.2001.4517

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  18 in total

1.  Reorientational dynamics of enzymes adsorbed on quartz: a temperature-dependent time-resolved TIRF anisotropy study.

Authors:  C Czeslik; C Royer; T Hazlett; W Mantulin
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

2.  What causes hyperfluorescence: folding intermediates or conformationally flexible native states?

Authors:  John Ervin; Edgar Larios; Szabolcs Osváth; Klaus Schulten; Martin Gruebele
Journal:  Biophys J       Date:  2002-07       Impact factor: 4.033

3.  Pressure denaturation of staphylococcal nuclease studied by neutron small-angle scattering and molecular simulation.

Authors:  Amit Paliwal; Dilipkumar Asthagiri; Dobrin P Bossev; Michael E Paulaitis
Journal:  Biophys J       Date:  2004-09-03       Impact factor: 4.033

4.  Unique features of the folding landscape of a repeat protein revealed by pressure perturbation.

Authors:  Jean-Baptiste Rouget; Martin A Schroer; Christoph Jeworrek; Matthias Pühse; Jean-Louis Saldana; Yannick Bessin; Metin Tolan; Doug Barrick; Roland Winter; Catherine A Royer
Journal:  Biophys J       Date:  2010-06-02       Impact factor: 4.033

5.  Simulations of the pressure and temperature unfolding of an alpha-helical peptide.

Authors:  Dietmar Paschek; S Gnanakaran; Angel E Garcia
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-30       Impact factor: 11.205

6.  Kinetic analysis of amyloid protofibril dissociation and volumetric properties of the transition state.

Authors:  Abdul Raziq Abdul Latif; Ryohei Kono; Hideki Tachibana; Kazuyuki Akasaka
Journal:  Biophys J       Date:  2006-09-22       Impact factor: 4.033

7.  An analysis of the molecular origin of osmolyte-dependent protein stability.

Authors:  Jörg Rösgen; B Montgomery Pettitt; David Wayne Bolen
Journal:  Protein Sci       Date:  2007-02-27       Impact factor: 6.725

8.  Putting the Piezolyte Hypothesis under Pressure.

Authors:  Christina M Papini; Pranav P Pandharipande; Catherine A Royer; George I Makhatadze
Journal:  Biophys J       Date:  2017-08-10       Impact factor: 4.033

Review 9.  Lessons from pressure denaturation of proteins.

Authors:  Julien Roche; Catherine A Royer
Journal:  J R Soc Interface       Date:  2018-10-03       Impact factor: 4.118

10.  Structural and thermodynamic characterization of T4 lysozyme mutants and the contribution of internal cavities to pressure denaturation.

Authors:  Nozomi Ando; Buz Barstow; Walter A Baase; Andrew Fields; Brian W Matthews; Sol M Gruner
Journal:  Biochemistry       Date:  2008-09-25       Impact factor: 3.162

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