Comparing the folding and misfolding energy landscapes of phosphoglycerate kinase.

ABSTRACT: Partitioning of polypeptides between protein folding and amyloid formation is of outstanding pathophysiological importance. Using yeast phosphoglycerate kinase as model, here we identify the features of the energy landscape that decide the fate of the protein: folding or amyloidogenesis. Structure formation was initiated from the acid-unfolded state, and monitored by fluorescence from 10 ms to 20 days. Solvent conditions were gradually shifted between folding and amyloidogenesis, and the properties of the energy landscape governing structure formation were reconstructed. A gradual transition of the energy landscape between folding and amyloid formation was observed. In the early steps of both folding and misfolding, the protein searches through a hierarchically structured energy landscape

SUBMITTER: Agocs G 

PROVIDER: S-EPMC3379013 | biostudies-literature | 2012 Jun

REPOSITORIES: biostudies-literature