Grant: Collaborative Health Research Projects
University of British Columbia
$115,850.00
Super-resolution microscopy network analysis: Drug target validation for cystic fibrosis
EF 2019-20
Résumé
The goal of genome-based precision medicine is to selectively target drugs to responsive patients. This is particularly important in cystic fibrosis (CF), where ~75% of eligible patients, carrying the F508del-CFTR mutation, do not show demonstrable improvement in lung function with the clinically-available drug Orkambi. Orkambi treatment costs >$250,000/yr and is not formally covered by publically funded health-care in Canada at this time. New drugs in phase 2 clinical trials may be more effective than others for individual patients. To identify which patients are most likely to benefit from CF modulator drugs, it is important to study CFTR at the protein level as patient-patient variation is not only dependent on genomicdifferences (e.g. specific CFTR mutations). We will apply machine learning based network analysis of single molecule localization super-resolution microscopy (SMLM) to develop an imaging-based assay to identify patients likely to benefit from a particular therapeutic. Optimization of therapies for individual patients will increase drug efficacy and substantiallyreduce cost of treatment for Canadian CF patients. SMLM generates resolution ten-fold beyond the diffraction limit. However, quantitative approaches to analyze the large data sets of 3D point localizations generated are limited. Wedeveloped a novel and powerful approach to model SMLM particle localization data sets, transforming 3D localizations into a network by virtual connections between the points. This approach allows us to determine molecular architecture, i.e. how proteins within a protein complex interact. We now propose to refine and apply the technology to CFTR and thereby validate our analysis pipeline for personalized medicine applications in CF and other diseases with a known drug target. We will partner with Quorum Technologies, a Canadian microscopy company, to commercialize the software for use by super-resolution microscopy users and pharmaceutical companies worldwide.
Programme
Collaborative Health Research Projects
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
538851-2019
Name nom
Nabi, Ivan
Department département
Cellular and Physiological Sciences
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
2019
Competition year année de concours
2019
Award amount
115850
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
RESEARCH PARTNERSHIPS
Group fr
PARTENARIATS DE RECHERCHE
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Installment
inst:1 - 1
Partie
1
Nb partie
1
Application title
Super-resolution microscopy network analysis: Drug target validation for cystic fibrosis
Keyword
NSERC
Application summary
The goal of genome-based precision medicine is to selectively target drugs to responsive patients. This is particularly important in cystic fibrosis (CF), where ~75% of eligible patients, carrying the F508del-CFTR mutation, do not show demonstrable improvement in lung function with the clinically-available drug Orkambi. Orkambi treatment costs >$250,000/yr and is not formally covered by publically funded health-care in Canada at this time. New drugs in phase 2 clinical trials may be more effective than others for individual patients. To identify which patients are most likely to benefit from CF modulator drugs, it is important to study CFTR at the protein level as patient-patient variation is not only dependent on genomicdifferences (e.g. specific CFTR mutations). We will apply machine learning based network analysis of single molecule localization super-resolution microscopy (SMLM) to develop an imaging-based assay to identify patients likely to benefit from a particular therapeutic. Optimization of therapies for individual patients will increase drug efficacy and substantiallyreduce cost of treatment for Canadian CF patients. SMLM generates resolution ten-fold beyond the diffraction limit. However, quantitative approaches to analyze the large data sets of 3D point localizations generated are limited. Wedeveloped a novel and powerful approach to model SMLM particle localization data sets, transforming 3D localizations into a network by virtual connections between the points. This approach allows us to determine molecular architecture, i.e. how proteins within a protein complex interact. We now propose to refine and apply the technology to CFTR and thereby validate our analysis pipeline for personalized medicine applications in CF and other diseases with a known drug target. We will partner with Quorum Technologies, a Canadian microscopy company, to commercialize the software for use by super-resolution microscopy users and pharmaceutical companies worldwide.