Grant: Collaborative Health Research Projects
University of British Columbia
$118,198.00
Microfluidic technologies for high-throughput monocIonal antibody selection from single cells
FY 2008-09
Summary
This project will bring together two research groups with complementary expertise led by Dr. John Schrader, a medically-trained, internationally recognized immunologist, and Dr. Carl Hansen a physicist and engineer who is a leader in innovation in the new science of microfluidics. Together these interdisciplinary teams will develop a novel and innovative device that will address a pivotal problem in basic and applied medical research - the rapid and inexpensive generation of high-value monoclonal antibodies. Monoclonal antibodies are counterparts of the antibodies in our blood that protect us from infections by binding to viruses or toxins and are responsible for immunity to diseases we have encountered before. Antibodies have the unique property thai they come in millions of different shapes. A "monoclonal antibody " is a pure preparation of one antibody with its one particular shape and different monoclonal antibodies can be selected to fight a virus or target a cancer. Monoclonal antibodies are the fastest growing class of new therapeutic agents and are providing breakthrough treatments e.g for cancers of the breast, colon, lymphatic tissues and others (Herceptin, Erbitux, Rituximab, Avastin) and arthritis and Crohn's disease (Remicade, Humira). The ability to find a monoclonal antibody that selectively binds to virtually any substance is also of enormous medical and commercial importance in the diagnosis of disease and in biomedical research. Despite this enormous potential, the discovery and production of high-quality antibodies by conventional means is a major bottleneck. Current techniques are expensive, require months or years of development, and are not compatible with the production of antibodies that can be easily used in humans. This project will merge state-of-the-art techniques in microengineering, immunology, and biophotonics to enable a postage stamp-size device to make sensitive measurements on the antibodies made by thousands of single cells and copy the genetic recipes for antibodies with useful characteristics, so that they can be made in unlimited quantities as human or rabbit monoclonal antibodies for use as therapies or as reagents. The results of the research should lead to exciting commercial opportunities.
Program
Collaborative Health Research Projects
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
351319-2008
Name nom
Schrader, John
Department département
Biomedical Research Centre (The)
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
2008
Competition year année de concours
2008
Award amount
118198
Program id
CHRPJ
Program nane en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
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
1206
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Engineering
Area of application fr
Génie
Research subject code
6400
Research subject group en
Life sciences research related to human health and disease
Research subject group fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Research subject en
Life sciences research related to human health and disease
Research subject fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Partie
1
Nb partie
3
Application title
Microfluidic technologies for high-throughput monocIonal antibody selection from single cells
Keyword
NA
Application summary
This project will bring together two research groups with complementary expertise led by Dr. John Schrader, a medically-trained, internationally recognized immunologist, and Dr. Carl Hansen a physicist and engineer who is a leader in innovation in the new science of microfluidics. Together these interdisciplinary teams will develop a novel and innovative device that will address a pivotal problem in basic and applied medical research - the rapid and inexpensive generation of high-value monoclonal antibodies. Monoclonal antibodies are counterparts of the antibodies in our blood that protect us from infections by binding to viruses or toxins and are responsible for immunity to diseases we have encountered before. Antibodies have the unique property thai they come in millions of different shapes. A "monoclonal antibody " is a pure preparation of one antibody with its one particular shape and different monoclonal antibodies can be selected to fight a virus or target a cancer. Monoclonal antibodies are the fastest growing class of new therapeutic agents and are providing breakthrough treatments e.g for cancers of the breast, colon, lymphatic tissues and others (Herceptin, Erbitux, Rituximab, Avastin) and arthritis and Crohn's disease (Remicade, Humira). The ability to find a monoclonal antibody that selectively binds to virtually any substance is also of enormous medical and commercial importance in the diagnosis of disease and in biomedical research. Despite this enormous potential, the discovery and production of high-quality antibodies by conventional means is a major bottleneck. Current techniques are expensive, require months or years of development, and are not compatible with the production of antibodies that can be easily used in humans. This project will merge state-of-the-art techniques in microengineering, immunology, and biophotonics to enable a postage stamp-size device to make sensitive measurements on the antibodies made by thousands of single cells and copy the genetic recipes for antibodies with useful characteristics, so that they can be made in unlimited quantities as human or rabbit monoclonal antibodies for use as therapies or as reagents. The results of the research should lead to exciting commercial opportunities.