Grant: Discovery Grants Program - Individual
University of British Columbia
$90,000.00
Protein mechanics and engineering at the single molecule level
EF 2014-15
Résumé
Elastomeric proteins are key elastic elements in a wide range of mechano-chemical machinery in cells, and can also function as structural materials of superb mechanical properties. Understanding the molecular design of elastomeric proteins is the key to understand the biophysical principles underlying various biological processes and to use these proteins as building blocks for the bottom-up construction of advanced materials and nanomechanical devices. We propose to combine single molecule atomic force microscopy with protein engineering, molecular dynamics simulations and traditional biophysical techniques to elucidate the physiochemical principles underlying the mechanical stability of proteins, to develop rational methodologies to design proteins with tunable mechanical properties and to engineer novel tandem-modular protein based biomaterials. We will focus our studies on a small protein GB1, one of the successful model proteins we screened for single protein mechanics studies. We will use single molecule AFM to measure the mechanical properties of proteins at the single molecule level and use site-directed mutagenesis to dissect the mechanical unfolding pathways and examine the roles of non-covalent interactions in determining the mechanical stability of proteins. Building upon our initial success in using engineered metal chelation to enhance the mechanical stability of GB1, we endeavor to develop the engineered metal chelation approach into a general and robust methodology for modulating the mechanical stability of diverse proteins in a rational and reversible fashion. Based on these well-characterized elastomeric proteins, we plan to engineer elastomeric protein-based biomaterials, such as chemically crosslinked hydrogels, to harness the mechanical properties engineered into individual elastomeric proteins in macroscopic biomaterials. These experimental efforts will serve as the first step towards using artificial elastomeric proteins as structural and functional building blocks for a variety of nanomechanical and material science applications.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
311603-2010
Name nom
Li, Hongbin
Department département
Chemistry
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2010
Award amount
90000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
1202
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Physical sciences
Area of application fr
Sciences physiques
Research subject code
3404
Research subject group en
Physical chemistry
Research subject group fr
Chimie physique
Research subject en
Biophysical chemistry
Research subject fr
Chimie biophysique
Partie
5
Nb partie
5
Application title
Protein mechanics and engineering at the single molecule level
Keyword
NSERC
Application summary
Elastomeric proteins are key elastic elements in a wide range of mechano-chemical machinery in cells, and can also function as structural materials of superb mechanical properties. Understanding the molecular design of elastomeric proteins is the key to understand the biophysical principles underlying various biological processes and to use these proteins as building blocks for the bottom-up construction of advanced materials and nanomechanical devices. We propose to combine single molecule atomic force microscopy with protein engineering, molecular dynamics simulations and traditional biophysical techniques to elucidate the physiochemical principles underlying the mechanical stability of proteins, to develop rational methodologies to design proteins with tunable mechanical properties and to engineer novel tandem-modular protein based biomaterials. We will focus our studies on a small protein GB1, one of the successful model proteins we screened for single protein mechanics studies. We will use single molecule AFM to measure the mechanical properties of proteins at the single molecule level and use site-directed mutagenesis to dissect the mechanical unfolding pathways and examine the roles of non-covalent interactions in determining the mechanical stability of proteins. Building upon our initial success in using engineered metal chelation to enhance the mechanical stability of GB1, we endeavor to develop the engineered metal chelation approach into a general and robust methodology for modulating the mechanical stability of diverse proteins in a rational and reversible fashion. Based on these well-characterized elastomeric proteins, we plan to engineer elastomeric protein-based biomaterials, such as chemically crosslinked hydrogels, to harness the mechanical properties engineered into individual elastomeric proteins in macroscopic biomaterials. These experimental efforts will serve as the first step towards using artificial elastomeric proteins as structural and functional building blocks for a variety of nanomechanical and material science applications.