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Effect of molecular confinement on internal enzyme dynamics: frequency domain fluorometry and molecular dynamics simulation studies
- Source :
- Biopolymers, 67 (2002): 85–95., info:cnr-pdr/source/autori:Bismuto E., Martelli P.L., De Maio A., Mita D.G., Irace G., Casadio R/titolo:Effect of molecular confinement on internal enzyme dynamics: Frequency domain fluorometry and molecular dynamics simulation studies/doi:/rivista:Biopolymers (Print)/anno:2002/pagina_da:85/pagina_a:95/intervallo_pagine:85–95/volume:67
- Publication Year :
- 2002
-
Abstract
- The tryptophanyl emission decay of the mesophilic beta-galactosidase from Aspergillus oryzae free in buffer and entrapped in agarose gel is investigated as a function of temperature and compared to that of the hyperthermophilic enzyme from Sulfolobus solfataricus. Both enzymes are tetrameric proteins with a large number of tryptophanyl residues, so the fluorescence emission can provide information on the conformational dynamics of the overall protein structure rather than that of the local environment. The tryptophanyl emission decays are best fitted by bimodal Lorentzian distributions. The long-lived component is ascribed to close, deeply buried tryptophanyl residues with reduced mobility; the short-lived one arises from tryptophanyl residues located in more flexible external regions of each subunit, some of which are involved in forming the catalytic site. The center of both lifetime distribution components at each temperature increases when going from the free in solution mesophilic enzyme to the gel-entrapped and hyperthermophilic enzyme, thus indicating that confinement of the mesophilic enzyme in the agarose gel limits the freedom of the polypeptide chain. A more complex dependence is observed for the distribution widths. Computer modeling techniques are used to recognize that the catalytic sites are similar for the mesophilic and hyperthermophilic beta-galactosidases. The effect due to gel entrapment is considered in dynamic simulations by imposing harmonic restraints to solvent-exposed atoms of the protein with the exclusion of those around the active site. The temperature dependence of the tryptophanyl fluorescence emission decay and the dynamic simulation confirm that more rigid structures, as in the case of the immobilized and/or hyperthermophilic enzyme, require higher temperatures to achieve the requisite conformational dynamics for an effective catalytic action and strongly suggest a link between conformational rigidity and enhanced thermal stability.
- Subjects :
- Immobilized enzyme
Aspergillus oryzae
ved/biology.organism_classification_rank.species
Kinetics
Biophysics
Biochemistry
Fluorescence spectroscopy
Biomaterials
Molecular dynamics
chemistry.chemical_compound
Protein structure
biology
Chemistry
ved/biology
Organic Chemistry
Sulfolobus solfataricus
Tryptophan
Active site
General Medicine
beta-Galactosidase
Crystallography
Spectrometry, Fluorescence
Chemical physics
biology.protein
Agarose
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Biopolymers, 67 (2002): 85–95., info:cnr-pdr/source/autori:Bismuto E., Martelli P.L., De Maio A., Mita D.G., Irace G., Casadio R/titolo:Effect of molecular confinement on internal enzyme dynamics: Frequency domain fluorometry and molecular dynamics simulation studies/doi:/rivista:Biopolymers (Print)/anno:2002/pagina_da:85/pagina_a:95/intervallo_pagine:85–95/volume:67
- Accession number :
- edsair.doi.dedup.....dc4efae1645d863008bbdd473caf15c9