Abstract

Significance In the interior of a cell, the volume accessible to each protein molecule is restricted by the presence of the large number of other macromolecules. Such a crowded environment is known to affect the stability and folding rates of proteins. In the case of intrinsically disordered proteins (IDPs), however, a class of proteins that lack stable structure, much less is known about the role of crowding effects. We have quantified the conformational changes occurring in IDPs in the presence of high concentrations of different polymers that act as crowding agents. Using single-molecule spectroscopy, we have identified effects that are typical of polymer solutions and have direct implications for the behavior of IDPs within the cell.