Literature DB >> 8599674

Characterizing the secondary hydration shell on hydrated myoglobin, hemoglobin, and lysozyme powders by its vitrification behavior on cooling and its calorimetric glass-->liquid transition and crystallization behavior on reheating.

G Sartor1, A Hallbrucker, E Mayer.   

Abstract

For hydrated metmyoglobin, methemoglobin, and lysozyme powders, the freezable water fraction of between approximately 0.3-0.4 g water/g protein up to approximately 0.7-0.8 g water/g protein has been fully vitrified by cooling at rates up to approximately 1500 K min-1 and the influence of cooling rate characterized by x-ray diffractograms. This vitreous but freezable water fraction started to crystallize at approximately 210 K to cubic ice and at approximately 240 K to hexagonal ice. Measurements by differential scanning calorimetry have shown that this vitreous but freezable water fraction undergoes, on reheating at a rate of 30 K min-1, a glass-->liquid transition with an onset temperature of between approximately 164 and approximately 174 K, with a width of between approximately 9 and approximately 16 degrees and an increase in heat capacity of between approximately 20 and approximately 40 J K-1 (mol of freezable water)-1 but that the glass transition disappears upon crystallization of the freezable water. These calorimetric features are similar to those of water imbibed in the pores of a synthetic hydrogel but very different from those of glassy bulk water. The difference to glassy bulk water's properties is attributed to hydrophilic interaction and H-bonding of the macromolecules' segments with the freezable water fraction, which thereby becomes dynamically modified. Abrupt increase in minimal or critical cooling rate necessary for complete vitrification is observed at approximately 0.7-0.8 g water/g protein, which is attributed to an abrupt increase of water's mobility, and it is remarkably close to the threshold value of water's mobility on a hydrated protein reported by Kimmich et al. (1990, Biophys. J. 58:1183). The hydration level of approximately 0.7-0.8 g water/g protein is approximately that necessary for completing the secondary hydration shell.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8599674      PMCID: PMC1236505          DOI: 10.1016/S0006-3495(95)80139-6

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  26 in total

1.  Limits of cryofixation as seen by Fourier transform infrared spectra of metmyoglobin azide and carbonyl hemoglobin in vitrified and freeze-concentrated aqueous solution.

Authors:  E Mayer; G Astl
Journal:  Ultramicroscopy       Date:  1992-09       Impact factor: 2.689

Review 2.  Protein-water interactions determined by dielectric methods.

Authors:  R Pethig
Journal:  Annu Rev Phys Chem       Date:  1992       Impact factor: 12.703

3.  Dynamic instability of liquidlike motions in a globular protein observed by inelastic neutron scattering.

Authors: 
Journal:  Phys Rev Lett       Date:  1990-08-20       Impact factor: 9.161

4.  Fluctuations, exchange processes, and water diffusion in aqueous protein systems: A study of bovine serum albumin by diverse NMR techniques.

Authors:  R Kimmich; T Gneiting; K Kotitschke; G Schnur
Journal:  Biophys J       Date:  1990-11       Impact factor: 4.033

5.  Order and disorder in water structure of crystalline proteins.

Authors:  M M Teeter
Journal:  Dev Biol Stand       Date:  1992

Review 6.  The properties of water in biological systems.

Authors:  R Cooke; I D Kuntz
Journal:  Annu Rev Biophys Bioeng       Date:  1974

7.  A global model of the protein-solvent interface.

Authors:  V Lounnas; B M Pettitt; G N Phillips
Journal:  Biophys J       Date:  1994-03       Impact factor: 4.033

8.  Thermal denaturation procedures for hemoglobin.

Authors:  K W Olsen
Journal:  Methods Enzymol       Date:  1994       Impact factor: 1.600

9.  Physical methods for the study of myoglobin.

Authors:  T M Rothgeb; F R Gurd
Journal:  Methods Enzymol       Date:  1978       Impact factor: 1.600

10.  Thermal properties of water in myoglobin crystals and solutions at subzero temperatures.

Authors:  W Doster; A Bachleitner; R Dunau; M Hiebl; E Lüscher
Journal:  Biophys J       Date:  1986-08       Impact factor: 4.033

View more
  15 in total

1.  Biomolecular cryocrystallography: structural changes during flash-cooling.

Authors:  Bertil Halle
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-29       Impact factor: 11.205

Review 2.  Low-temperature behavior of water confined by biological macromolecules and its relation to protein dynamics.

Authors:  M Weik
Journal:  Eur Phys J E Soft Matter       Date:  2003-09       Impact factor: 1.890

3.  Effect of common cryoprotectants on critical warming rates and ice formation in aqueous solutions.

Authors:  Jesse B Hopkins; Ryan Badeau; Matthew Warkentin; Robert E Thorne
Journal:  Cryobiology       Date:  2012-06-19       Impact factor: 2.487

4.  Low-temperature glass transitions of quenched and annealed bovine serum albumin aqueous solutions.

Authors:  Kiyoshi Kawai; Toru Suzuki; Masaharu Oguni
Journal:  Biophys J       Date:  2006-02-24       Impact factor: 4.033

5.  Dynamics of apomyoglobin in the alpha-to-beta transition and of partially unfolded aggregated protein.

Authors:  E Fabiani; A M Stadler; D Madern; M M Koza; M Tehei; M Hirai; G Zaccai
Journal:  Eur Biophys J       Date:  2008-10-14       Impact factor: 1.733

6.  Slow cooling of protein crystals.

Authors:  Matthew Warkentin; Robert E Thorne
Journal:  J Appl Crystallogr       Date:  2009-08-01       Impact factor: 3.304

7.  THz time scale structural rearrangements and binding modes in lysozyme-ligand interactions.

Authors:  K N Woods
Journal:  J Biol Phys       Date:  2014-03-30       Impact factor: 1.365

8.  Liquid-like water confined in stacks of biological membranes at 200 k and its relation to protein dynamics.

Authors:  M Weik; U Lehnert; G Zaccai
Journal:  Biophys J       Date:  2005-07-29       Impact factor: 4.033

9.  Slow cooling and temperature-controlled protein crystallography.

Authors:  Matthew Warkentin; Robert E Thorne
Journal:  J Struct Funct Genomics       Date:  2009-12-10

10.  Using THz Spectroscopy, Evolutionary Network Analysis Methods, and MD Simulation to Map the Evolution of Allosteric Communication Pathways in c-Type Lysozymes.

Authors:  Kristina N Woods; Juergen Pfeffer
Journal:  Mol Biol Evol       Date:  2015-09-03       Impact factor: 16.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.