TY - JOUR
T1 - Cell-free protein expression from DNA-based hydrogel (P-Gel) droplets for scale-up production
AU - Ruiz, Roanna C.H.
AU - Kiatwuthinon, Pichamon
AU - Kahn, Jason S.
AU - Roh, Young Hoon
AU - Luo, Dan
PY - 2012/12/1
Y1 - 2012/12/1
N2 - This paper presents a promising potential scale-up method for cell-free protein production that integrates microfluidic devices and DNA-based hydrogels (P-gels). The microfluidic devices were fabricated using established photolithography techniques. The P-gels were formed via enzymatic ligation of branched DNA nanostructures with genes. More specifically, the microfluidic devices contained droplet-forming junctions through which numerous micron-sized P-gel droplets were produced. The advantages of our microfluidic-based approach include highly controlled fluid manipulation, rapid droplet generation, high reproducibility, and low sample consumption. P-gel droplets successfully expressed green fluorescent protein (GFP) in high yield, and the microfluidic devices achieved a variety of P-gel droplet sizes while maintaining uniform morphology and a high generation rate. We envision that our system could provide a cell-free platform for both high-throughput and scale-up production of multiple proteins.
AB - This paper presents a promising potential scale-up method for cell-free protein production that integrates microfluidic devices and DNA-based hydrogels (P-gels). The microfluidic devices were fabricated using established photolithography techniques. The P-gels were formed via enzymatic ligation of branched DNA nanostructures with genes. More specifically, the microfluidic devices contained droplet-forming junctions through which numerous micron-sized P-gel droplets were produced. The advantages of our microfluidic-based approach include highly controlled fluid manipulation, rapid droplet generation, high reproducibility, and low sample consumption. P-gel droplets successfully expressed green fluorescent protein (GFP) in high yield, and the microfluidic devices achieved a variety of P-gel droplet sizes while maintaining uniform morphology and a high generation rate. We envision that our system could provide a cell-free platform for both high-throughput and scale-up production of multiple proteins.
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U2 - 10.1089/ind.2012.0024
DO - 10.1089/ind.2012.0024
M3 - Article
AN - SCOPUS:84871392340
SN - 1550-9087
VL - 8
SP - 372
EP - 377
JO - Industrial Biotechnology
JF - Industrial Biotechnology
IS - 6
ER -