Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractExoskeleton formation in Apis mellifera: cuticular hydrocarbons profiles and expression of desaturase and elongase genes during pupal and adult development    Next AbstractComparison of headspace techniques for sampling volatile natural products in a dynamic system »

Lab Chip


Title:High-throughput tracking of single yeast cells in a microfluidic imaging matrix
Author(s):Falconnet D; Niemisto A; Taylor RJ; Ricicova M; Galitski T; Shmulevich I; Hansen CL;
Address:"University of British Columbia, Center for High-Throughput Biology, 2185 East Mall, Vancouver, BC, Canada V6T-1Z4"
Journal Title:Lab Chip
Year:2011
Volume:20101118
Issue:3
Page Number:466 - 473
DOI: 10.1039/c0lc00228c
ISSN/ISBN:1473-0189 (Electronic) 1473-0197 (Print) 1473-0189 (Linking)
Abstract:"Time-lapse live cell imaging is a powerful tool for studying signaling network dynamics and complexity and is uniquely suited to single cell studies of response dynamics, noise, and heritable differences. Although conventional imaging formats have the temporal and spatial resolution needed for such studies, they do not provide the simultaneous advantages of cell tracking, experimental throughput, and precise chemical control. This is particularly problematic for system-level studies using non-adherent model organisms such as yeast, where the motion of cells complicates tracking and where large-scale analysis under a variety of genetic and chemical perturbations is desired. We present here a high-throughput microfluidic imaging system capable of tracking single cells over multiple generations in 128 simultaneous experiments with programmable and precise chemical control. High-resolution imaging and robust cell tracking are achieved through immobilization of yeast cells using a combination of mechanical clamping and polymerization in an agarose gel. The channel and valve architecture of our device allows for the formation of a matrix of 128 integrated agarose gel pads, each allowing for an independent imaging experiment with fully programmable medium exchange via diffusion. We demonstrate our system in the combinatorial and quantitative analysis of the yeast pheromone signaling response across 8 genotypes and 16 conditions, and show that lineage-dependent effects contribute to observed variability at stimulation conditions near the critical threshold for cellular decision making"
Keywords:Algorithms Diffusion Dimethylpolysiloxanes/chemistry High-Throughput Screening Assays Immobilization/*methods Lab-On-A-Chip Devices Microfluidics/*instrumentation/*methods Nylons/chemistry Polymerization Saccharomyces cerevisiae/*cytology Signal Transduct;
Notes:"MedlineFalconnet, D Niemisto, A Taylor, R J Ricicova, M Galitski, T Shmulevich, I Hansen, C L eng P50 GM076547/GM/NIGMS NIH HHS/ R21 EB005757/EB/NIBIB NIH HHS/ P50 GM076547-05S1/GM/NIGMS NIH HHS/ R21 EB005757-01/EB/NIBIB NIH HHS/ P50GM076547/GM/NIGMS NIH HHS/ MOP-93571/CAPMC/CIHR/Canada Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't England 2010/11/23 Lab Chip. 2011 Feb 7; 11(3):466-73. doi: 10.1039/c0lc00228c. Epub 2010 Nov 18"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024