A fast and flexible PEG-mediated transient expression system in plants for high level expression of secreted recombinant proteins

被引:21
作者
Baur, A
Kaufmann, F
Rolli, H
Weise, A
Luethje, R
Berg, B
Braun, M
Baeumer, W
Kietzmann, M
Reski, R
Gorr, G
机构
[1] Greenovat Biotech GmbH, D-79111 Freiburg, Germany
[2] Univ Freiburg, Fac Biol, D-79104 Freiburg, Germany
[3] Univ Vet Med Hannover, Dept Pharmacol Toxicol & Pharm, D-30559 Hannover, Germany
关键词
transient expression; PEG-mediated transformation; signal peptide; recombinant human vascular endothelial growth factors; Physcomitrella patens;
D O I
10.1016/j.jbiotec.2005.04.018
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Plant expression systems offer a valuable alternative to traditional systems for the production of recombinant biopharmaceuticals. A highly efficient polyethyleneglycol (PEG)-mediated transient expression system for secreted recombinant proteins in plants has been developed. The human vascular endothelial growth factor 121 (rhVEGF) has been successfully expressed and efficiently secreted into the culture medium by transiently transformed moss, protoplasts, In order to obtain secretion efficiency data, different expressed signal peptides were analysed and time Course Studies were performed with expression constructs containing different promoters. The transformation procedure was optimised for high level expression (up to 10 mu g/ml) and successfully performed even with a transgenic glyco-engineered strain lacking plant-specific immunogenic sugar residues in N-glycans. The amount of rhVEGF was produced in such quantity that it allowed for the analysis of biological activity, silver-staining and Western blotting, revealing the correct formation and processing of the homodimer. This fast and flexible transient expression system enables feasibility studies and construct optimisation to be concluded within it few day,;, thus avoiding the time consuming step of having to generate stably transformed lines. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:332 / 342
页数:11
相关论文
共 33 条
[1]   Use of β-glueuronidase reporter gene for gene expression analysis in turfgrasses [J].
Basu, C ;
Kausch, AP ;
Chandlee, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (01) :7-10
[2]   The moss bioreactor [J].
Decker, EL ;
Reski, R .
CURRENT OPINION IN PLANT BIOLOGY, 2004, 7 (02) :166-170
[3]   THE EXTENSIN SIGNAL PEPTIDE ALLOWS SECRETION OF A HETEROLOGOUS PROTEIN FROM PROTOPLASTS [J].
DELOOSE, M ;
GHEYSEN, G ;
TIRE, C ;
GIELEN, J ;
VILLARROEL, R ;
GENETELLO, C ;
VANMONTAGU, M ;
DEPICKER, A ;
INZE, D .
GENE, 1991, 99 (01) :95-100
[4]   PROTEIN SECRETION IN PLANT-CELLS CAN OCCUR VIA A DEFAULT PATHWAY [J].
DENECKE, J ;
BOTTERMAN, J ;
DEBLAERE, R .
PLANT CELL, 1990, 2 (01) :51-59
[5]   The biology of vascular endothelial growth factor [J].
Ferrara, N ;
DavisSmyth, T .
ENDOCRINE REVIEWS, 1997, 18 (01) :4-25
[6]  
Fischer R, 1999, BIOTECHNOL APPL BIOC, V30, P113
[7]   Plant-based production of biopharmaceuticals [J].
Fischer, R ;
Stoger, E ;
Schillberg, S ;
Christou, P ;
Twyman, RM .
CURRENT OPINION IN PLANT BIOLOGY, 2004, 7 (02) :152-158
[8]  
Fuentes A, 2004, BIOTECHNOL APPL BIOC, V39, P355, DOI 10.1042/BA20030192
[9]   Role of complex asparagine-linked glycans in the allergenicity of plant glycoproteins [J].
GarciaCasado, G ;
SanchezMonge, R ;
Chrispeels, MJ ;
Armentia, A ;
Salcedo, G ;
Gomez, L .
GLYCOBIOLOGY, 1996, 6 (04) :471-477
[10]   TRANSIENT PLANT GENE-EXPRESSION - A SIMPLE AND REPRODUCIBLE METHOD BASED ON FLOWING PARTICLE GUN [J].
GODON, C ;
CABOCHE, M ;
DANIELVEDELE, F .
BIOCHIMIE, 1993, 75 (07) :591-595