Literature DB >> 8527683

Modified spectrophotometer for multi-dimensional circular dichroism/fluorescence data acquisition in titration experiments: application to the pH and guanidine-HCI induced unfolding of apomyoglobin.

G Ramsay1, R Ionescu, M R Eftink.   

Abstract

In a previous paper (Ramsay and Eftink, Biophys. J. 66:516-523) we reported the development of a modified spectrophotometer that can make nearly simultaneous circular dichroism (CD) and fluorescence measurements. This arrangement allows multiple data sets to be collected during a single experiment, resulting in a saving of time and material, and improved correlation between the different types of measurements. The usefulness of the instrument was shown by thermal melting experiments on several different protein systems. This CD/fluorometer spectrophotometer has been further modified by interfacing with a syringe pump and a pH meter. This arrangement allows ligand, pH, and chemical denaturation titration experiments to be performed while monitoring changes in the sample's CD, absorbance, fluorescence, and light scattering properties. Our data acquisition program also has an ability to check whether the signals have approached equilibrium before the data is recorded. For performing pH titrations we have developed a procedure which uses the signal from a pH meter in a feedback circuit in order to collect data at evenly spaced pH intervals. We demonstrate the use of this instrument with studies of the unfolding of sperm whale apomyoglobin, as induced by acid pH and by the addition of guanidine-HCI.

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Year:  1995        PMID: 8527683      PMCID: PMC1236294          DOI: 10.1016/S0006-3495(95)79945-3

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


  13 in total

1.  Emission and polarization spectrometer for biophysical spectroscopy.

Authors:  J C Sutherland; G D Cimino; J T Lowe
Journal:  Rev Sci Instrum       Date:  1976-03       Impact factor: 1.523

2.  Equilibrium evidence of non-single step transition during guanidine unfolding of apomyoglobins.

Authors:  C Balestrieri; G Colonna; A Giovane; G Irace; L Servillo
Journal:  FEBS Lett       Date:  1976-07-01       Impact factor: 4.124

3.  Residual structure in large fragments of staphylococcal nuclease: effects of amino acid substitutions.

Authors:  D Shortle; A K Meeker
Journal:  Biochemistry       Date:  1989-02-07       Impact factor: 3.162

4.  Aggregation and denaturation of apomyoglobin in aqueous urea solutions.

Authors:  L R De Young; K A Dill; A L Fink
Journal:  Biochemistry       Date:  1993-04-20       Impact factor: 3.162

5.  A multidimensional spectrophotometer for monitoring thermal unfolding transitions of macromolecules.

Authors:  G Ramsay; M R Eftink
Journal:  Biophys J       Date:  1994-02       Impact factor: 4.033

6.  The unfolding of trp aporepressor as a function of pH: evidence for an unfolding intermediate.

Authors:  M R Eftink; K J Helton; A Beavers; G D Ramsay
Journal:  Biochemistry       Date:  1994-08-30       Impact factor: 3.162

7.  Multidimensional spectroscopic data correlation in the conformation transition of biological macromolecules.

Authors:  A Wada; H Tachibana; H Hayashi; Y Saito
Journal:  J Biochem Biophys Methods       Date:  1980-05

8.  Folding of staphylococcal nuclease A studied by equilibrium and kinetic circular dichroism spectra.

Authors:  T Sugawara; K Kuwajima; S Sugai
Journal:  Biochemistry       Date:  1991-03-12       Impact factor: 3.162

9.  Molecular mechanisms of acid denaturation. The role of histidine residues in the partial unfolding of apomyoglobin.

Authors:  D Barrick; F M Hughson; R L Baldwin
Journal:  J Mol Biol       Date:  1994-04-15       Impact factor: 5.469

10.  Tryptophanyl fluorescence heterogeneity of apomyoglobins. Correlation with the presence of two distinct structural domains.

Authors:  G Irace; C Balestrieri; G Parlato; L Servillo; G Colonna
Journal:  Biochemistry       Date:  1981-02-17       Impact factor: 3.162

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  3 in total

1.  Active-site sulfhydryl chemistry plays a major role in the misfolding of urea-denatured rhodanese.

Authors:  M Panda; P M Horowitz
Journal:  J Protein Chem       Date:  2000-07

2.  Role of heme in the unfolding and assembly of myoglobin.

Authors:  David S Culbertson; John S Olson
Journal:  Biochemistry       Date:  2010-07-27       Impact factor: 3.162

3.  Biosynthetic incorporation of tryptophan analogues into staphylococcal nuclease: effect of 5-hydroxytryptophan and 7-azatryptophan on structure and stability.

Authors:  C Y Wong; M R Eftink
Journal:  Protein Sci       Date:  1997-03       Impact factor: 6.725

  3 in total

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