4.7 Article

EMMA: An Extensible Mammalian Modular Assembly Toolkit for the Rapid Design and Production of Diverse Expression Vectors

期刊

ACS SYNTHETIC BIOLOGY
卷 6, 期 7, 页码 1380-1392

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.7b00016

关键词

mammalian synthetic biology; mammalian expression vectors; DNA assembly; combinatorial assembly

资金

  1. University of Edinburgh
  2. SULSA
  3. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/M025640/1]
  4. Engineering and Physical Sciences Research Council (EPSRC) [IAA J273I2]
  5. BBSRC UK mammalian Synthetic biology centre [BB/M018040/1]
  6. BBSRC [BB/M005690/2, BB/M018040/1, BB/M025640/1, BB/M005690/1] Funding Source: UKRI
  7. EPSRC [EP/P017401/1] Funding Source: UKRI
  8. MRC [MR/K017047/1] Funding Source: UKRI
  9. Biotechnology and Biological Sciences Research Council [BB/M005690/1, BBS/OS/GC/000001, BB/M025640/1, BB/M005690/2, BB/M018040/1] Funding Source: researchfish
  10. Cancer Research UK [17368] Funding Source: researchfish
  11. Engineering and Physical Sciences Research Council [EP/P017401/1] Funding Source: researchfish
  12. Medical Research Council [MR/K017047/1] Funding Source: researchfish
  13. The Brain Tumour Charity [8/105] Funding Source: researchfish

向作者/读者索取更多资源

Mammalian plasmid expression vectors are critical reagents underpinning many facets of research across biology, biomedical research, and the biotechnology industry. Traditional cloning methods often require laborious manual design and assembly of plasmids using tailored sequential cloning steps. This process can be protracted, complicated, expensive, and error-prone. New tools and strategies that facilitate the efficient design and production of bespoke vectors would help relieve a current bottleneck for researchers. To address this, we have developed an extensible mammalian modular assembly kit (EMMA). This enables rapid and efficient modular assembly of mammalian expression vectors in a one-tube, one-step golden-gate cloning reaction, using a standardized library of compatible genetic parts. The high modularity, flexibility, and extensibility of EMMA provide a simple method for the production of functionally diverse mammalian expression vectors. We demonstrate the value of this toolkit by constructing and validating a range of representative vectors, such as transient and stable expression vectors (transposon based vectors), targeting vectors, inducible systems, polycistronic expression cassettes, fusion proteins, and fluorescent reporters. The method also supports simple assembly combinatorial libraries and hierarchical assembly for production of larger multigenetic cargos. In summary, EMMA is compatible with automated production, and novel genetic parts can be easily incorporated, providing new opportunities for mammalian synthetic biology.

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