The marginal stability of globular proteins in the cell is determined by the balance between excluded volume effect and soft interactions. Quinary interactions are a type of soft interactions involved in intracellular organisation and known to have stabilising or destabilising effects on globular proteins. Recent studies suggest that globular proteins have structural flexibility, exhibiting more than one functional state. Here, we propose that the quinary-induced destabilisation can be sufficient to produce functional partially unfolded states of globular proteins. The biological relevance of this mechanism is explored, involving intracellular phase separation and regulatory stress response mechanisms.The authors thank Hernani Geros for use...
Much of our current knowledge of biological chemistry is founded in the structure-function relatio...
There are four well-known levels of protein structure: primary (amino acid sequence), secondary (hel...
Intrinsically disordered proteins and protein regions (IDPs) represent around thirty percent of the ...
Globular proteins perform many of the chemical reactions required for life. The prevailing model of ...
Most knowledge of protein chemistry is derived from experiments performed in dilute, buffered soluti...
The vast majority of our current knowledge about the biochemical and biophysical properties of prote...
The vast majority of our current knowledge about the biochemical and biophysical properties of prote...
The description of protein folding pathways and the principles that govern them has proven to be one...
In cells, proteins are embedded in a crowded environment that controls their properties via manifold...
The intracellular milieu is filled with small molecules, nucleic acids, lipids and proteins. Theorie...
This work aims to analytically understand the impact of two diametric opposite environments on prote...
The intracellular milieu is complex, heterogeneous and crowded-- an environment vastly different fro...
The formation of insoluble deposits by globular proteins underlies the onset of many human diseases....
Phase separation has long been observed within aqueous mixtures of two or more different compounds, ...
Proteins perform their function in cells where macromolecular solutes reach concentrations of >300 g...
Much of our current knowledge of biological chemistry is founded in the structure-function relatio...
There are four well-known levels of protein structure: primary (amino acid sequence), secondary (hel...
Intrinsically disordered proteins and protein regions (IDPs) represent around thirty percent of the ...
Globular proteins perform many of the chemical reactions required for life. The prevailing model of ...
Most knowledge of protein chemistry is derived from experiments performed in dilute, buffered soluti...
The vast majority of our current knowledge about the biochemical and biophysical properties of prote...
The vast majority of our current knowledge about the biochemical and biophysical properties of prote...
The description of protein folding pathways and the principles that govern them has proven to be one...
In cells, proteins are embedded in a crowded environment that controls their properties via manifold...
The intracellular milieu is filled with small molecules, nucleic acids, lipids and proteins. Theorie...
This work aims to analytically understand the impact of two diametric opposite environments on prote...
The intracellular milieu is complex, heterogeneous and crowded-- an environment vastly different fro...
The formation of insoluble deposits by globular proteins underlies the onset of many human diseases....
Phase separation has long been observed within aqueous mixtures of two or more different compounds, ...
Proteins perform their function in cells where macromolecular solutes reach concentrations of >300 g...
Much of our current knowledge of biological chemistry is founded in the structure-function relatio...
There are four well-known levels of protein structure: primary (amino acid sequence), secondary (hel...
Intrinsically disordered proteins and protein regions (IDPs) represent around thirty percent of the ...