Grant: Alliance Grants
Carleton University
$100,000.00
Systematic development of novel peptide-derived inhibitors for methyl-regulatory enzymes
EF 2021-22
Résumé
Through a direct partnership with Zim Corp. and their subsidiary Nuvobio, a local Ottawa-based company with interest in molecular tools and peptide inhibitors, this proposal will allow the partner organization to efficiently design and commercialize cell-active and target-specific inhibitors. The development of these commercialized resources will enable the broader study of protein function and the deconvolution of cellular processes. As protein dysfunction is commonly hallmarked as critical drivers of disease progression, Zim has recognized that there is an urgent need to develop strategies that can be used to study basic protein biology. As a result, there is a need for the development of tools that are necessary to study protein function in a cellular context. Through research enabled by our collaborative effort, we will be able to spark growth in novel, peptide-centric biotechnology products that will ultimately benefit Canadians and the Canadian economy. This initial collaborative work will focus on the generation of peptide-inhibitors for two classes of proteins that regulate a chemical protein modification referred to as lysine methylation, specifically, lysine methyltransferase (KMT) and demethylase (KDM) enzymes. Lysine methylation has emerged in the last decade as a protein modification with expanding implications in a number of cellular processes, and the dysfunction of several KMT and KDMs are known drivers of cancer. Given the involvement of Lys methylation in a growing number of different biological processes, perhaps it is not surprising that the study of methylation events has been increasingly important in understanding basic cellular biology. As a result, there is a great interest to understand the biology of these methyl-regulatory enzymes, however, only a handful of KMT and KDM inhibitors have been discovered or developed. This collaboration addresses this issue and represents a significant effort towards expanding the commercial market of KMT and KDM inhibitors. The goal of this proposed NSERC Alliance collaborative research program is to develop target-specific peptide inhibitors of KMT and KDM enzymes as tools for the study of the methyl-Lys proteome.
Programme
Alliance Grants
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
555589-2020
Name nom
Biggar, Kyle
Department département
Biochemistry, Institute of
Organization id
23
Institution établissement
Carleton University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2021
Competition year année de concours
2020
Award amount
100000
Program id
ALLRP
Program name en
Alliance Grants
Program name fr
Subventions Alliance
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5403
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Proteins and peptides, amino acids
Research subject fr
Protéines et peptides, acides aminés
Installment
inst:2
Partie
1
Nb partie
2
Application title
Systematic development of novel peptide-derived inhibitors for methyl-regulatory enzymes
Keyword
NSERC
Application summary
Through a direct partnership with Zim Corp. and their subsidiary Nuvobio, a local Ottawa-based company with interest in molecular tools and peptide inhibitors, this proposal will allow the partner organization to efficiently design and commercialize cell-active and target-specific inhibitors. The development of these commercialized resources will enable the broader study of protein function and the deconvolution of cellular processes. As protein dysfunction is commonly hallmarked as critical drivers of disease progression, Zim has recognized that there is an urgent need to develop strategies that can be used to study basic protein biology. As a result, there is a need for the development of tools that are necessary to study protein function in a cellular context. Through research enabled by our collaborative effort, we will be able to spark growth in novel, peptide-centric biotechnology products that will ultimately benefit Canadians and the Canadian economy. This initial collaborative work will focus on the generation of peptide-inhibitors for two classes of proteins that regulate a chemical protein modification referred to as lysine methylation, specifically, lysine methyltransferase (KMT) and demethylase (KDM) enzymes. Lysine methylation has emerged in the last decade as a protein modification with expanding implications in a number of cellular processes, and the dysfunction of several KMT and KDMs are known drivers of cancer. Given the involvement of Lys methylation in a growing number of different biological processes, perhaps it is not surprising that the study of methylation events has been increasingly important in understanding basic cellular biology. As a result, there is a great interest to understand the biology of these methyl-regulatory enzymes, however, only a handful of KMT and KDM inhibitors have been discovered or developed. This collaboration addresses this issue and represents a significant effort towards expanding the commercial market of KMT and KDM inhibitors. The goal of this proposed NSERC Alliance collaborative research program is to develop target-specific peptide inhibitors of KMT and KDM enzymes as tools for the study of the methyl-Lys proteome.