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Merck
CN
  • Design and construction of an in-plant activation cassette for transgene expression and recombinant protein production in plants.

Design and construction of an in-plant activation cassette for transgene expression and recombinant protein production in plants.

Nature protocols (2014-04-08)
Benjamin Dugdale, Cara L Mortimer, Maiko Kato, Tess A James, Robert M Harding, James L Dale
摘要

Virus-based transgene expression systems have become particularly valuable for recombinant protein production in plants. The dual-module in-plant activation (INPACT) expression platform consists of a uniquely designed split-gene cassette incorporating the cis replication elements of Tobacco yellow dwarf geminivirus (TYDV) and an ethanol-inducible activation cassette encoding the TYDV Rep and RepA replication-associated proteins. The INPACT system is essentially tailored for recombinant protein production in stably transformed plants and provides both inducible and high-level transient transgene expression with the potential to be adapted to diverse crop species. The construction of a novel split-gene cassette, the inducible nature of the system and the ability to amplify transgene expression via rolling-circle replication differentiates this system from other DNA- and RNA-based virus vector systems used for stable or transient recombinant protein production in plants. Here we provide a detailed protocol describing the design and construction of a split-gene INPACT cassette, and we highlight factors that may influence optimal activation and amplification of gene expression in transgenic plants. By using Nicotiana tabacum, the protocol takes 6-9 months to complete, and recombinant proteins expressed using INPACT can accumulate to up to 10% of the leaf total soluble protein.

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Sigma-Aldrich
甘氨酸, suitable for electrophoresis, ≥99%
Roche
PCR DIG 探针合成试剂盒, sufficient for 25 reaction (50 μL final reaction volume)
Roche
抗 地高辛, from mouse IgG1κ (clone 1.71.256)