Grant: Discovery Grants Program - Individual
Université d'Ottawa
$92,000.00
Interrogating and Manipulating Biological Material at Small Scales
FY 2024-25
Summary
Advances in the development of novel biophysical analytical capabilities provide access to new insight into the biological condition of living systems. Our ability to manipulate fluids at the micro- and the nano-scales is allowing us to conceive of new analytical devices that utilize remarkable small-scale phenomena in mitigating some of the issues found in conventional sensing platforms. In the last decade, nanopore sensors have emerged as one of the most promising next-generation analytical tools given their ability to analyze biological samples with single-molecule sensitivity. Solid-state nanopores are synthetic analogs to the biological pores found in cell membranes. These nanopores are nanofluidic channels that allow the translocation of single biomolecules, such as DNA, RNA and proteins, from one side of a membrane to the other. When used as sensors, we can monitor the ionic current through such nanopores in order to gain a wealth of physical and chemical information about the translocating molecule. In addition to its use in DNA sequencing, this concept exhibits great promise in other applications including disease diagnostics and the study of single-cell signaling.
Recently, we discovered an approach to integrating such nanopore sensors within microfluidic networks. This has opened the door to the development of portable lab-on-a-chip analytical platforms that can accommodate real-world samples, by offering on-chip sample processing capabilities (filtering, mixing, pre-concentrating, etc.) upstream of the nanopore sensor. Intriguingly, nanopore performance is altered when confined within microchannels. In this Discovery program, we will investigate the mass transport phenomena that occur near the nanopores when integrated within microchannels, and use these results to tune sensor performance. Also, we will use our ability to trap picolitre-scale samples near the nanopore to enable the accurate quantification of biomolecular concentration, and this platform will enable the study of cell signaling at the single cell level. These discoveries will lead to the development of new analytical platforms that will greatly broaden disease diagnostic capabilities by enabling the analysis of ultra-low concentration biomarkers, while also providing insight into the biology of single cells.
The knowledge acquired and the technologies developed over this DG cycle could potentially secure a global competitive edge for the Canadian biomedical sector. Our work provides a path towards the development of point-of-care diagnostics platforms that could greatly enhance our ability to track disease. Moreover, the associated interdisciplinary training will undoubtedly provide students (HQP) with a broad skillset in science and engineering while focusing on single-molecule techniques, which are in growing demand in Canada's high-tech industry.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2020-05012
Name nom
Godin, Michel
Department département
Physics - Physique
Organization id
28
Institution établissement
Université d'Ottawa
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2020
Award amount
92000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1512
Committee name en
Mechanical Engineering
Committee name fr
Génie mécanique
Area of application code
1102
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
3113
Research subject group en
Physics
Research subject group fr
Physique
Research subject en
Biophysics
Research subject fr
Biophysique
Field of research list names en
Not available
Field of research list names fr
Non disponible
Socioeconomic objective list names en
Not available
Socioeconomic objective list names fr
Non disponible
Application title
Interrogating and Manipulating Biological Material at Small Scales
Keywords
microfluidics; biosensors; microfabrication; biomaterials; disease diagnostics; therapeutic cells; nanopore sensors; analytical tools; dna assay; biomedical instrumentation
Application summary
Advances in the development of novel biophysical analytical capabilities provide access to new insight into the biological condition of living systems. Our ability to manipulate fluids at the micro- and the nano-scales is allowing us to conceive of new analytical devices that utilize remarkable small-scale phenomena in mitigating some of the issues found in conventional sensing platforms. In the last decade, nanopore sensors have emerged as one of the most promising next-generation analytical tools given their ability to analyze biological samples with single-molecule sensitivity. Solid-state nanopores are synthetic analogs to the biological pores found in cell membranes. These nanopores are nanofluidic channels that allow the translocation of single biomolecules, such as DNA, RNA and proteins, from one side of a membrane to the other. When used as sensors, we can monitor the ionic current through such nanopores in order to gain a wealth of physical and chemical information about the translocating molecule. In addition to its use in DNA sequencing, this concept exhibits great promise in other applications including disease diagnostics and the study of single-cell signaling.
Recently, we discovered an approach to integrating such nanopore sensors within microfluidic networks. This has opened the door to the development of portable lab-on-a-chip analytical platforms that can accommodate real-world samples, by offering on-chip sample processing capabilities (filtering, mixing, pre-concentrating, etc.) upstream of the nanopore sensor. Intriguingly, nanopore performance is altered when confined within microchannels. In this Discovery program, we will investigate the mass transport phenomena that occur near the nanopores when integrated within microchannels, and use these results to tune sensor performance. Also, we will use our ability to trap picolitre-scale samples near the nanopore to enable the accurate quantification of biomolecular concentration, and this platform will enable the study of cell signaling at the single cell level. These discoveries will lead to the development of new analytical platforms that will greatly broaden disease diagnostic capabilities by enabling the analysis of ultra-low concentration biomarkers, while also providing insight into the biology of single cells.
The knowledge acquired and the technologies developed over this DG cycle could potentially secure a global competitive edge for the Canadian biomedical sector. Our work provides a path towards the development of point-of-care diagnostics platforms that could greatly enhance our ability to track disease. Moreover, the associated interdisciplinary training will undoubtedly provide students (HQP) with a broad skillset in science and engineering while focusing on single-molecule techniques, which are in growing demand in Canada's high-tech industry.