| Keyword search (4,164 papers available) | ![]() |
"Potvin-Trottier L" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | A Bacteroides synthetic biology toolkit to build an in vivo malabsorption biosensor | McCallum G; Burckhardt JC; He J; Hong A; Potvin-Trottier L; Tropini C; | 41610848 BIOLOGY |
| 2 | Exploiting fluctuations in gene expression to detect causal interactions between genes | Joly-Smith E; Talpur MM; Allard P; Papazotos F; Potvin-Trottier L; Hilfinger A; | 41401079 BIOLOGY |
| 3 | Open-space microfluidics as a tool to study signaling dynamics | Proulx M; Clapperton-Richard P; Potvin-Trottier L; Piekny A; Gervais T; | 40995884 BIOLOGY |
| 4 | Measuring prion propagation in single bacteria elucidates mechanism of loss | Jager K; Orozco-Hidalgo MT; Springstein BL; Joly-Smith E; Papazotos F; McDonough E; Fleming E; McCallum G; Hilfinger A; Hochschild A; Potvin-Trottier L; | 36712035 BIOLOGY |
| 5 | Measuring prion propagation in single bacteria elucidates a mechanism of loss | Jager K; Orozco-Hidalgo MT; Springstein BL; Joly-Smith E; Papazotos F; McDonough E; Fleming E; McCallum G; Yuan AH; Hilfinger A; Hochschild A; Potvin-Trottier L; | 37738299 PHYSICS |
| 6 | Microfluidics for long-term single-cell time-lapse microscopy: Advances and applications | Allard P; Papazotos F; Potvin-Trottier L; | 36312536 BIOLOGY |
| 7 | Using Models to (Re-)Design Synthetic Circuits. | McCallum G, Potvin-Trottier L | 33405217 BIOLOGY |
| 8 | Isolating live cells after high-throughput, long-term, time-lapse microscopy. | Luro S, Potvin-Trottier L, Okumus B, Paulsson J | 31768062 BIOLOGY |
| 9 | Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator. | Riglar DT, Richmond DL, Potvin-Trottier L, Verdegaal AA, Naydich AD, Bakshi S, Leoncini E, Lyon LG, Paulsson J, Silver PA | 31604953 BIOLOGY |
| Title: | Microfluidics for long-term single-cell time-lapse microscopy: Advances and applications | ||||
| Authors: | Allard P, Papazotos F, Potvin-Trottier L | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/36312536/ | ||||
| DOI: | 10.3389/fbioe.2022.968342 | ||||
| Publication: | Frontiers in bioengineering and biotechnology | ||||
| Keywords: | cell screening; cellular dynamics; microfluidics; phenotypic heterogeneity; single-cell analysis; time-lapse microscopy; | ||||
| PMID: | 36312536 | Category: | Date Added: | 2022-10-31 | |
| Dept Affiliation: |
BIOLOGY
1 Department of Biology, Concordia University, Montréal, QC, Canada. 2 Department of Physics, Concordia University, Montréal, QC, Canada. 3 Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, Canada. |
||||
Description: |
Cells are inherently dynamic, whether they are responding to environmental conditions or simply at equilibrium, with biomolecules constantly being made and destroyed. Due to their small volumes, the chemical reactions inside cells are stochastic, such that genetically identical cells display heterogeneous behaviors and gene expression profiles. Studying these dynamic processes is challenging, but the development of microfluidic methods enabling the tracking of individual prokaryotic cells with microscopy over long time periods under controlled growth conditions has led to many discoveries. This review focuses on the recent developments of one such microfluidic device nicknamed the mother machine. We overview the original device design, experimental setup, and challenges associated with this platform. We then describe recent methods for analyzing experiments using automated image segmentation and tracking. We further discuss modifications to the experimental setup that allow for time-varying environmental control, replicating batch culture conditions, cell screening based on their dynamic behaviors, and to accommodate a variety of microbial species. Finally, this review highlights the discoveries enabled by this technology in diverse fields, such as cell-size control, genetic mutations, cellular aging, and synthetic biology. |



