Keyword search (4,163 papers available)

"Soffer G" Authored Publications:

Title Authors PubMed ID
1 Expanding the limits towards 'one-pot' DNA assembly and transformation on a rapid-prototype microfluidic device Perry JM; Soffer G; Jain R; Shih SCC; 34369550
BIOLOGY
2 Real-Time Optogenetics System for Controlling Gene Expression Using a Model-Based Design. Soffer G, Perry JM, Shih SCC 33543619
BIOLOGY
3 One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation. Samlali K, Ahmadi F, Quach ABV, Soffer G, Shih SCC 32705796
BIOLOGY
4 Integration of World-to-Chip Interfaces with Digital Microfluidics for Bacterial Transformation and Enzymatic Assays. Moazami E, Perry JM, Soffer G, Husser MC, Shih SCC 30945840
ENCS

 

Title:Expanding the limits towards 'one-pot' DNA assembly and transformation on a rapid-prototype microfluidic device
Authors:Perry JMSoffer GJain RShih SCC
Link:pubmed.ncbi.nlm.nih.gov/34369550/
DOI:10.1039/d1lc00415h
Publication:Lab on a chip
Keywords:
PMID:34369550 Category: Date Added:2021-08-09
Dept Affiliation: BIOLOGY
1 Department of Biology, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada. steve.shih@concordia.ca and Department of Electrical and Computer Engineering, Concordia University, 1455 de Maisonneuve Blvd. West, Montréal, Québec H3G 1M8, Canada.
2 Department of Electrical and Computer Engineering, Concordia University, 1455 de Maisonneuve Blvd. West, Montréal, Québec H3G 1M8, Canada and Centre for Applied Synthetic Biology, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada.
3 Department of Biology, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada. steve.shih@concordia.ca and Department of Electrical and Computer Engineering, Concordia University, 1455 de Maisonneuve Blvd. West, Montréal, Québec H3G 1M8, Canada and Centre for Applied Synthetic Biology, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada.

Description:

DNA assembly and transformation are crucial to the building process in synthetic biology. These steps are significant roadblocks when engineering increasingly complex biological systems. To address this, recent development of widespread 'biofoundry' facilities has employed automation equipment to expedite the synthetic biology workflow. Despite significant progress, there is a clear demand for lower-cost and smaller-footprint automation equipment. The field of microfluidics have emerged to provide automation capabilities to meet this demand. However, we still lack devices capable of building large multi-gene systems in a consolidated process. In response to this challenge, we have developed a digital microfluidic platform that performs "one-pot" Golden Gate DNA assembly of large plasmids and transformation of E coli. The system features a novel electrode geometry and modular design, which make these devices simple to fabricate and use, thus improving the accessibility of microfluidics. This device incorporates an impedance-based adaptive closed loop water replenishment system to compensate for droplet evaporation and maintain constant assembly reaction concentrations, which we found to be crucial to the DNA assembly efficiency. We also showcase a closed-loop temperature control system that generates precise thermodynamic profiles to optimize heat shock transformation. Moreover, we validated the system by assembling and transforming large and complex plasmids conferring a biosynthetic pathway, resulting in performance comparable to those of standard techniques. We propose that the methods described here will contribute to a new generation of accessible automation platforms aimed at speeding up the 'building' process, lowering reagent consumption and removing manual work from synthetic biology.




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