Determining the temperature at which the thermal unfolding of a protein starts becoming irreversible is relevant for many areas of protein research. Until now, published methods cannot determine, within a reasonable time frame and with moderate sample consumption, the exposure temperature that starts causing irreversible protein unfolding. We present modulated scanning fluorimetry (MSF) and share a software (MSF Analyzer), which can be used to derive nonreversibility curves of thermal protein unfolding from a series of incremental temperature cycles performed on only 10 μL samples, consuming as low as a few micrograms of protein. Further processing of the data can yield the onset temperature that starts causing nonreversible protein unfoldi...
As the focus of biological research expands beyond traditional enzymatic activities, protein apparen...
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation...
Conformational stability of a protein is usually obtained by spectroscopically measuring the unfoldi...
In biotherapeutic protein research, an estimation of the studied protein's thermal stability is one ...
Various stability indicating techniques find application in the early stage development of novel the...
Various stability indicating techniques find application in the early stage development of novel the...
The effect of protein stability on kinetic function is monitored with many techniques that often req...
Various stability indicating techniques find application in the early stage development of novel the...
Various stability indicating techniques find application in the early stage development of novel the...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
Various stability indicating techniques find application in the early stage development of novel the...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
We present a high-throughput approach to help define experimental formulations that enhance protein ...
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation...
As the focus of biological research expands beyond traditional enzymatic activities, protein apparen...
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation...
Conformational stability of a protein is usually obtained by spectroscopically measuring the unfoldi...
In biotherapeutic protein research, an estimation of the studied protein's thermal stability is one ...
Various stability indicating techniques find application in the early stage development of novel the...
Various stability indicating techniques find application in the early stage development of novel the...
The effect of protein stability on kinetic function is monitored with many techniques that often req...
Various stability indicating techniques find application in the early stage development of novel the...
Various stability indicating techniques find application in the early stage development of novel the...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
Various stability indicating techniques find application in the early stage development of novel the...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
Studies of protein unfolding mechanisms are critical for understanding protein functions inside cell...
We present a high-throughput approach to help define experimental formulations that enhance protein ...
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation...
As the focus of biological research expands beyond traditional enzymatic activities, protein apparen...
DSC analysis has been used to quantify the reversibility of unfolding following thermal denaturation...
Conformational stability of a protein is usually obtained by spectroscopically measuring the unfoldi...