Simulated pressure denaturation thermodynamics of ubiquitin.

ABSTRACT: Simulations of protein thermodynamics are generally difficult to perform and provide limited information. It is desirable to increase the degree of detail provided by simulation and thereby the potential insight into the thermodynamic properties of proteins. In this study, we outline how to analyze simulation trajectories to decompose conformation-specific, parameter free, thermodynamically defined protein volumes into residue-based contributions. The total volumes are obtained using established methods from Fluctuation Solution Theory, while the volume decomposition is new and is performed using a simple proximity method. Native and fully extended ubiquitin are used as the test conformations. Changes in the protein volumes are then followed as a function of pressure, allowing for conforma

SUBMITTER: Ploetz EA 

PROVIDER: S-EPMC5656550 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature