Blumlein, Alice and McManus, Jennifer
(2013)
Reversible and non-reversible thermal denaturation of lysozyme with
varying pH at low ionic strength.
Biochimica et Biophysica Acta - Proteins and Proteomics, 1834 (10).
pp. 2064-2070.
ISSN 1570-9639
Abstract
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation of lysozyme.
Since the temperature at which protein unfolding occurs, Tm, varies with different solution conditions,
the effect on the melting temperature and the degree of refolding after thermal denaturation in low ionic
strength sodium phosphate buffers (5–1000 mM) over a range of pH (5–9) in the presence/absence of disaccharides
is examined. This study compares the enthalpies of unfolding during successive heating cycles to
quantify reversibility following thermal denaturation. The disaccharides, trehalose and maltose were used
to assess if the disaccharide induced increase in Tm is reflected in the reversibility of thermally induced denaturation.
There was extensive overlap between the Tm values where non-reversible and reversible thermal
denaturation occurred. Indeed, for pH 6, at the highest and lowest Tm, no refolding was observed whereas
refolding was observed for intermediate values, but with similar Tm values having different proportions of
refolded protein. We established a method to measure the degree of reversible unfolding following thermal
denaturation and hence indirectly, the degree to which protein is lost to irreversible aggregation, and show
that solution conditions which increase melt transition temperatures do not automatically confer an increase
in reversibility. This type of analysis may prove useful in assessing the stability of proteins in both the biopharmaceutical
and food industries.
Item Type: |
Article
|
Keywords: |
Protein aggregation; Denaturation; Refolding; Differential scanning calorimetry; Lysozyme; |
Academic Unit: |
Faculty of Science and Engineering > Chemistry |
Item ID: |
7756 |
Identification Number: |
https://doi.org/10.1016/j.bbapap.2013.06.001 |
Depositing User: |
Jennifer McManus
|
Date Deposited: |
13 Jan 2017 17:01 |
Journal or Publication Title: |
Biochimica et Biophysica Acta - Proteins and Proteomics |
Publisher: |
Elsevier |
Refereed: |
Yes |
Funders: |
Science Foundation Ireland (SFI) |
URI: |
|
Use Licence: |
This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available
here |
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