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Role of Confinement and Material Surface on Protein Dynamics and Function


EMSL Project ID
46701

Abstract

Our goal is to develop a mechanistic understanding of optimal material properties that would permit the functional stabilization of broad classes of proteins with utility to a range of detection and decontamination applications. Current approaches aimed at preserving enzyme function following immobilization on solid supports rely on trial-and-error protocols that do not address how material properties affect protein structure and dynamics, with the result that general principles have not been formulated to enable the deployment of enzyme catalysts to mediate the detection or decontamination of a range of threat agents. We propose to use advanced fluorescence spectroscopy and both solution and solid state NMR methods to measure how material properties affect catalytically important domain motions following protein immobilization, explicitly addressing how adsorption, chemical cross-linking, and protein tethering methods affect the structure, dynamics, and function of ten well-characterized proteins. Protein domain motions will be measured using newly developed molecular probes that bind rigidly to the protein backbone that reflect domain motions. NMR spectroscopy will provide complementary information regarding smaller scale motions, i.e., protein secondary structure and side chain motions. Experimentally, measured domain motions and enzyme function will be directly compared with molecular dynamics simulations that explicitly take into account material properties and diffusion of substrates to active sites, thus providing a predictive understanding of the physical properties that need to be preserved in developing new materials for enzyme immobilization. The high-field NMR instruments at EMSL will be essential to the success of the project because of the large size of the proteins involved. WSU Tri-Cities does not have any NMR spectrometers.

Project Details

Project type
Limited Scope
Start Date
2012-01-27
End Date
2012-03-28
Status
Closed

Team

Principal Investigator

Kathleen McAteer
Institution
Washington State University Tri-Cities

Team Members

Brenda Beech
Institution
Washington State University Tri-Cities

Danny Mitchell
Institution
Washington State University Tri-Cities

Yijia Xiong
Institution
Western University of Health Sciences

Cheryl Baird
Institution
Pacific Northwest National Laboratory

Diana Bigelow
Institution
Pacific Northwest National Laboratory

Thomas Squier
Institution
Western University of Health Sciences