High-level expression of anti FLAG tag antibody in plants.
- Author:
Zhicheng KONG
1
;
Xiaoran XIONG
1
;
Chuan WU
2
;
Weisong PAN
1
Author Information
- Publication Type:Journal Article
- Keywords: molecular farming; plant bioreactor; protein purification; recombinant protein
- MeSH: Animals; Mice; Antibodies; Nicotiana/genetics*; Agrobacterium/genetics*; Bioreactors; Blotting, Western
- From: Chinese Journal of Biotechnology 2024;40(1):269-279
- CountryChina
- Language:Chinese
- Abstract: Plant bioreactor is a new production platform for expression of recombinant protein, which is one of the cores of molecular farming. In this study, the anti DYKDDDDK (FLAG) antibody was recombinantly expressed in tobacco (Nicotiana benthamiana) and purified. FLAG antibody with high affinity was obtained after immunizing mice for several times and its sequence was determined. Based on this, virus vectors expressing heavy chain (HC) and light chain (LC) inoculated into Nicotiana benthamiana leaves by using Agrobacterium-mediated delivery. Accumulation of the HC and LC was analyzed by SDS/PAGE followed by Western blotting probed with specific antibodies from 2 to 9 days postinfiltration (dpi). Accumulation of the FLAG antibody displayed at 3 dpi, and reached a maximum at 5 dpi. It was estimated that 66 mg of antibody per kilogram of fresh leaves could be obtained. After separation and purification, the antibody was concentrated to 1 mg/mL. The 1:10 000 diluted antibody can probe with 1 ng/mL FLAG fused antigen well, indicating the high affinity of the FLAG antibody produced in plants. In conclusion, the plant bioreactor is able to produce high affinity FLAG antibodies, with the characteristics of simplicity, low cost and highly added value, which contains enormous potential for the rapid and abundant biosynthesis of antibodies.
