Self-assembly of a multimeric genomic hydrogel via multi-primed chain reaction of dual single-stranded circular plasmids for cell-free protein production
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作者:
Nam, Hyangsu
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Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South KoreaUniv Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Nam, Hyangsu
[1
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Kim, Taehyeon
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Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South KoreaUniv Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Kim, Taehyeon
[1
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Moon, Sunghyun
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Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South KoreaUniv Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Moon, Sunghyun
[1
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Ji, Yoonbin
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Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South KoreaUniv Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Ji, Yoonbin
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Lee, Jong Bum
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Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South KoreaUniv Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Lee, Jong Bum
[1
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[1] Univ Seoul, Dept Chem Engn, 163 Seoulsiripdaero, Seoul 02504, South Korea
Recent technical advances in cell-free protein synthesis (CFPS) offer several advantages over cell-based expression systems, including the application of cellular machinery, such as transcription and translation, in the test tube. Inspired by the advantages of CFPS, we have fabricated a multimeric genomic DNA hydrogel (mGD-gel) via rolling circle chain amplification (RCCA) using dual single-stranded circular plasmids with multiple primers. The mGD-gel exhibited significantly enhanced protein yield. In addition, mGD-gel can be reused at least five times, and the shape of the mGD-gel can be easily manipulated without losing the feasibility of protein expression. The mGD-gel platform based on the self-assembly of multimeric genomic DNA strands (mGD strands) has the potential to be used in CFPS systems for a variety of biotechnological applications.