Literature DB >> 10233087

Dehydration and crystallization of trehalose and sucrose glasses containing carbonmonoxy-myoglobin.

F Librizzi1, E Vitrano, L Cordone.   

Abstract

We report a study wherein we contemporarily measured 1) the dehydration process of trehalose or sucrose glasses embedding carbonmonoxy-myoglobin (MbCO) and 2) the evolution of the A substates in saccharide-coated MbCO. Our results indicate that microcrystallization processes, sizeably different in the two saccharides, take place during dehydration; moreover, the microcrystalline structure is maintained unless the dry samples are equilibrated with a humidity >/=75% (>/=60%) at 25 degrees C for the trehalose (sucrose) sample. The evolution of the parameters that characterize the A substates of MbCO indicates that 1) the effects of water withdrawal are analogous in samples dried in the presence or in the absence of sugars, although much larger effects are observed in the samples without sugar; 2) the distribution of A substates is determined by the overall matrix structure and not only by the sample water content; and 3) the population of A0 substate (i. e., the substate currently put in relation with MbCO molecules having the distal histidine out of the heme pocket) is largely enhanced during the dehydration process. However, after rehumidification its population is largely decreased with respect to the values obtained, at similar water content, during the first dehydration run.

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Year:  1999        PMID: 10233087      PMCID: PMC1300242          DOI: 10.1016/S0006-3495(99)77425-4

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


  23 in total

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Authors:  A Di Pace; A Cupane; M Leone; E Vitrano; L Cordone
Journal:  Biophys J       Date:  1992-08       Impact factor: 4.033

2.  Spectroscopic evidence for conformational relaxation in myoglobin.

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Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-01       Impact factor: 11.205

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Journal:  Biophys J       Date:  1993-08       Impact factor: 4.033

5.  Resonance raman investigations of site-directed mutants of myoglobin: effects of distal histidine replacement.

Authors:  D Morikis; P M Champion; B A Springer; S G Sligar
Journal:  Biochemistry       Date:  1989-05-30       Impact factor: 3.162

6.  Dynamical transition of myoglobin revealed by inelastic neutron scattering.

Authors:  W Doster; S Cusack; W Petry
Journal:  Nature       Date:  1989-02-23       Impact factor: 49.962

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Authors:  J R Mourant; D P Braunstein; K Chu; H Frauenfelder; G U Nienhaus; P Ormos; R D Young
Journal:  Biophys J       Date:  1993-10       Impact factor: 4.033

8.  FTIR spectroscopic study of the dynamics of conformational substates in hydrated carbonyl-myoglobin films via temperature dependence of the CO stretching band parameters.

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Journal:  Biophys J       Date:  1994-08       Impact factor: 4.033

9.  Structure, dynamics, and reactivity in hemoglobin.

Authors:  J M Friedman
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Authors:  A Ansari; J Berendzen; D Braunstein; B R Cowen; H Frauenfelder; M K Hong; I E Iben; J B Johnson; P Ormos; T B Sauke
Journal:  Biophys Chem       Date:  1987-05-09       Impact factor: 2.352

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4.  Role of solvent on protein-matrix coupling in MbCO embedded in water-saccharide systems: a Fourier transform infrared spectroscopy study.

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Journal:  Biophys J       Date:  2006-05-19       Impact factor: 4.033

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6.  Protein in sugar films and in glycerol/water as examined by infrared spectroscopy and by the fluorescence and phosphorescence of tryptophan.

Authors:  Wayne W Wright; Gregory T Guffanti; Jane M Vanderkooi
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7.  Biophysical evaluation of aminoclay as an effective protectant for protein stabilization during freeze-drying and storage.

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9.  Structural Comparison between Sucrose and Trehalose in Aqueous Solution.

Authors:  Christoffer Olsson; Jan Swenson
Journal:  J Phys Chem B       Date:  2020-04-03       Impact factor: 2.991

  9 in total

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