TY - JOUR
T1 - Continuous-flow C. elegans fluorescence expression analysis with real-time image processing through microfluidics
AU - Yan, Yuanjun
AU - Boey, Daryl
AU - Ng, Li Theng
AU - Gruber, Jan
AU - Bettiol, Andrew
AU - Thakor, Nitish V.
AU - Chen, Chia Hung
N1 - Funding Information:
The project is supported by the Singapore Institute for Neurotechnology (SINAPSE), whose sponsors include A*STAR and Mindef . We also thank the Ministry of Education of Singapore (Grant MOE2010-T2-2-048 and MOE2012-T2-003) for financial support (Grant MOE2010-T2-2-048 and MOE2012-T2-2-003 ), MediaTek MOH IAF Tier-1 ( R-397-000-230-511 ) and the Caenorhabditis Genetics Centre for the provision of worm strains.
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2016/3/15
Y1 - 2016/3/15
N2 - The nematode Caenorhabditis elegans has become an essential model organism in neuroscience research because of its stereotyped anatomy, relevance to human biology, and capacity for genetic manipulation. To solve the intrinsic challenges associated with performing manual operations on C. elegans, many automated chip designs based on immobilization-imaging-release approaches have been proposed. These designs are prone to limitations such as the exertion of physical stress on the worms and limited throughput. In this work, a continuous-flow, high-throughput, automated C. elegans analyzer based on droplet encapsulation and real-time image processing was developed to analyze fluorescence expression in worms. To demonstrate its capabilities, two strains of C. elegans nematodes with different levels of expression of green fluorescent protein (GFP) were first mixed in a buffer solution. The worms were encapsulated in water-in-oil droplets to restrict random locomotion. The droplets were closely packed in a two-layer polydimethylsiloxane (PDMS) platform and were flowed through a narrow straight channel, in which a region of interest (ROI) was defined and continuously recorded by a frame acquisition device. Based on the number of pixels counted in the selected color range, our custom software analyzed GFP expression to differentiate between two strains with nearly 100% accuracy and a throughput of 0.5. seconds/worm.
AB - The nematode Caenorhabditis elegans has become an essential model organism in neuroscience research because of its stereotyped anatomy, relevance to human biology, and capacity for genetic manipulation. To solve the intrinsic challenges associated with performing manual operations on C. elegans, many automated chip designs based on immobilization-imaging-release approaches have been proposed. These designs are prone to limitations such as the exertion of physical stress on the worms and limited throughput. In this work, a continuous-flow, high-throughput, automated C. elegans analyzer based on droplet encapsulation and real-time image processing was developed to analyze fluorescence expression in worms. To demonstrate its capabilities, two strains of C. elegans nematodes with different levels of expression of green fluorescent protein (GFP) were first mixed in a buffer solution. The worms were encapsulated in water-in-oil droplets to restrict random locomotion. The droplets were closely packed in a two-layer polydimethylsiloxane (PDMS) platform and were flowed through a narrow straight channel, in which a region of interest (ROI) was defined and continuously recorded by a frame acquisition device. Based on the number of pixels counted in the selected color range, our custom software analyzed GFP expression to differentiate between two strains with nearly 100% accuracy and a throughput of 0.5. seconds/worm.
KW - C. elegans
KW - Continuous flow microfluidics
KW - Fluorescence expression assay
KW - In vivo screening
KW - Real time image analysis
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U2 - 10.1016/j.bios.2015.09.045
DO - 10.1016/j.bios.2015.09.045
M3 - Article
C2 - 26452079
AN - SCOPUS:84943592607
SN - 0956-5663
VL - 77
SP - 428
EP - 434
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -