This program advances an innovative approach that directly quantifies the impact of material properties on protein folding stability in situ at sub-micron spatial resolution and at millisecond time resolution. A major challenge in engineering hybrid biomaterials with protein components is that many materials contribute to substantial losses of protein activity, with significant commercial, scientific, and clinical ramifications. A major roadblock to solving this problem is the inability to quantify in situ the material properties that preserve or shut down protein function. This program will develop a dynamic fluorescence imaging approach, Fast Relaxation Imaging (FReI) that promises to overcome this roadblock and open the door to novel investigations of protein-material interactions, at the protein level. This program builds on our recent demonstration that FReI measurements are able to quantify protein folding stability in polyacrylamide hydrogels. We now seek to extend this approach to studies of biomedically relevant proteins and materials.
Specific Aim 1 will test the capacity to identify physical chemical mechanisms by which materials perturb protein stability and function, by using two-dimensional substrates of controlled surface chemistry.
Specific Aim 2 will extend studies to encapsulated proteins in three-dimensional alginate hydrogels, which are extensively used for drug delivery and tissue engineering. Outcomes from this program and anticipated subsequent research will lay the foundation for generating new molecular level design rules for robust, functional biomaterials with bio-macromolecular components.

Public Health Relevance

The goals of this two year program is to advance an innovative fluorescence imaging approach to quantify protein-folding stability in functional materials at sub-micron spatial resolution and millisecond time resolution. This technology will enable us to uniquely address address the long-standing challenge of identifying material properties that enhance or shut down protein function in functional materials used in biomedical and clinical applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21GM131425-01
Application #
9645411
Study Section
Biomaterials and Biointerfaces Study Section (BMBI)
Program Officer
Mcguirl, Michele
Project Start
2019-03-01
Project End
2021-02-28
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820