Production of human vitronectin in Nicotiana benthamiana using the INPACT hyperexpression platform
Autor: | Mark D. Harrison, James L. Dale, Robert M. Harding, Robyn Lloyd, Manuel R. Plan, Maiko Kato, Benjamin Dugdale, Terry Walsh, Pradeep C. Deo |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0106 biological sciences
0301 basic medicine biopharming Nicotiana benthamiana INPACT Plant Science Biology 01 natural sciences 03 medical and health sciences Tissue culture Gene Expression Regulation Plant inducible Tobacco Humans Vitronectin Cell adhesion Research Articles Activator (genetics) Cell adhesion molecule food and beverages biology.organism_classification Plants Genetically Modified Molecular biology 030104 developmental biology biology.protein Expression cassette Tomato bushy stunt virus transgene expression Agronomy and Crop Science 010606 plant biology & botany Biotechnology Research Article |
Zdroj: | Plant Biotechnology Journal |
ISSN: | 1467-7652 1467-7644 |
Popis: | Summary Human vitronectin (hVN) is a glycoprotein that functions as a cell adhesion molecule and a regulator of coagulation in blood plasma and the extracellular matrix. In vitro, hVN is added to serum‐free media in order to promote the adhesion of animal cells to tissue culture surfaces and the proliferation of undifferentiated stem cells. Here, we report the production of hVN in Nicotiana benthamiana using the inducible In Plant ACTivation (INPACT) hyperexpression platform. N. benthamiana plants were transformed with an INPACT expression cassette encoding hVN, and both the Tobacco yellow dwarf virus Rep/RepA activator and Tomato bushy stunt virus p19 gene under the transcriptional control of the ethanol‐inducible AlcR:alcA gene switch. hVN expression was maximal 4–5 days postactivation of the INPACT platform with a dilute ethanol solution, and crude yields of the recombinant protein reached a maximum of 643 ± 78 mg/kg fresh weight. A three‐stage purification protocol was developed using heparin and polyhistidine tag affinity binding and size exclusion filtration, resulting in a plant‐made hVN product of >90% purity. Storage conditions for plant‐made hVN were identified that maximized the capacity of the recombinant protein to promote cell adhesion. Critically, plant‐made hVN was shown to be functionally equivalent to commercial, plasma‐derived hVN at promoting one‐half maximal attachment of murine fibroblast cells (BALB‐C/3T3) in serum‐free medium at |
Databáze: | OpenAIRE |
Externí odkaz: |