Non-pathogenic trypanosomatid protozoa as a platform for protein research and production

被引:121
作者
Breitling, R
Klingner, S
Callewaert, N
Pietrucha, R
Geyer, A
Ehrlich, G
Hartung, R
Müller, A
Contreras, R
Beverley, SM
Alexandrov, K
机构
[1] Max Planck Inst Mol Physiol, Dept Phys Biochem, D-44227 Dortmund, Germany
[2] JenaBiosci GmbH, D-07749 Jena, Germany
[3] Univ Ghent, Dept Mol Biomed Res, B-9000 Ghent, Belgium
[4] Flanders Interuniv Inst Biotechnol, B-9000 Ghent, Belgium
[5] Klinikum FSU, Kinderklin, D-00745 Jena, Germany
[6] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
关键词
D O I
10.1016/S1046-5928(02)00001-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
All currently existing eukaryotic protein expression systems are based on autonomous life forms. To exploit the potential practical benefits associated with parasitic organisms we have developed a new protein expression system based on Leishmania tarentolae (Trypanosomatidae), a protozoan parasite of lizards. To achieve strong transcription, the genes of interest were integrated into the small subunit ribosomal RNA gene. Expression levels obtained were up to 30mg of recombinant protein per liter of suspension culture and increased linearly with the number of integrated gene copies. To assess the system's potential for production of post-translationally modified proteins, we have expressed human erythropoietin in L. tarentolae. The recombinant protein isolated from the culture supernatants was biologically active, natively processed at the N-terminus, and N-glycosylated. The N-glycosylation was exceptionally homogenous, with a mammalian-type biantennary oligosaccharide and the Man(3)GlcNAc(2) core structure accounting for >90% of the glycans present. L. tarentolae is thus the first described biotechnologically useful unicellular eukaryotic organism producing biantennary fully galactosylated, core-alpha-1,6-fucosylated N-glycans. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:209 / 218
页数:10
相关论文
共 26 条
[1]  
ANNABLE L, 1972, B WORLD HEALTH ORGAN, V47, P99
[2]  
BELEN CM, 2000, INFECT IMMUN, V68, P2728
[3]  
Beverley S M, 1993, Methods Mol Biol, V21, P333
[4]   Ultrasensitive profiling and sequencing of N-linked oligosaccharides using standard DNA-sequencing equipment [J].
Callewaert, N ;
Geysens, S ;
Molemans, P ;
Contreras, R .
GLYCOBIOLOGY, 2001, 11 (04) :275-281
[5]   Genetic manipulation of kinetoplastida [J].
Clayton, CE .
PARASITOLOGY TODAY, 1999, 15 (09) :372-378
[6]   The surface glycoconjugates of trypanosomatid parasites [J].
Ferguson, MAJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1997, 352 (1359) :1295-1302
[7]  
Grafte S, 1998, AM J HEMATOL, V58, P183, DOI 10.1002/(SICI)1096-8652(199807)58:3<183::AID-AJH4>3.0.CO
[8]  
2-N
[9]   STRUCTURAL-ANALYSIS OF THE SIALYLATED N-LINKED AND O-LINKED CARBOHYDRATE CHAINS OF RECOMBINANT-HUMAN-ERYTHROPOIETIN EXPRESSED IN CHINESE-HAMSTER OVARY CELLS - SIALYLATION PATTERNS AND BRANCH LOCATION OF DIMERIC N-ACETYLLACTOSAMINE UNITS [J].
HOKKE, CH ;
BERGWERFF, AA ;
VANDEDEM, GWK ;
KAMERLING, JP ;
VLIEGENTHART, JFG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 228 (03) :981-1008
[10]  
KOBATA A, 1994, METHOD ENZYMOL, V230, P200