Construction and deconstruction of bacterial inclusion bodies

被引:195
作者
Carrió, MM
Villaverde, A [1 ]
机构
[1] Univ Autonoma Barcelona, Inst Biotecnol & Biomed, E-08193 Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Genet & Microbiol, E-08193 Barcelona, Spain
关键词
chaperones; Escherichia coli; IbpA; IbpB; inclusion bodies; protein aggregation; refolding; recombinant protein;
D O I
10.1016/S0168-1656(02)00032-9
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
Bacterial inclusion bodies (IBs) are refractile aggregates of protease-resistant misfolded protein that often occur in recombinant bacteria upon gratuitous overexpression of cloned genes. In biotechnology, the formation of IBs represents a main obstacle for protein production since even favouring high protein yields, the in vitro recovery of functional protein from insoluble deposits depends on technically diverse and often complex re-folding procedures. On the other hand, IBs represent an exciting model to approach the in vivo analysis of protein folding and to explore aggregation dynamics. Recent findings on the molecular organisation of embodied polypeptides and on the kinetics of inclusion body formation have revealed an unexpected dynamism of these protein aggregates, from which polypeptides are steadily released in living cells to be further refolded or degraded. The close connection between in vivo protein folding, aggregation, solubilisation and proteolytic digestion offers an integrated view of the bacterial protein quality control system of which IBs might be an important component especially in recombinant bacteria. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 12
页数:10
相关论文
共 111 条
[31]   High-level expression of soluble heterologous proteins in the cytoplasm of Escherichia coli by fusion to the bacteriophage Lambda head protein D [J].
Forrer, P ;
Jaussi, R .
GENE, 1998, 224 (1-2) :45-52
[32]   Expression of correctly folded proteins in Escherichia coli [J].
Georgiou, G ;
Valax, P .
CURRENT OPINION IN BIOTECHNOLOGY, 1996, 7 (02) :190-197
[33]   LOCALIZATION OF INCLUSION-BODIES IN ESCHERICHIA-COLI OVERPRODUCING BETA-LACTAMASE OR ALKALINE-PHOSPHATASE [J].
GEORGIOU, G ;
TELFORD, JN ;
SHULER, ML ;
WILSON, DB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1986, 52 (05) :1157-1161
[34]  
Georgiou G, 1999, METHOD ENZYMOL, V309, P48
[35]  
Gilbert Hiram F., 1994, Current Opinion in Biotechnology, V5, P534, DOI 10.1016/0958-1669(94)90070-1
[36]   A Comparative Study of Global Stress Gene Regulation in Response to Overexpression of Recombinant Proteins in Escherichia coli [J].
Gill, R. T. ;
Valdes, J. J. ;
Bentley, W. E. .
METABOLIC ENGINEERING, 2000, 2 (03) :178-189
[37]  
Gill RT, 2001, BIOTECHNOL BIOENG, V72, P85, DOI 10.1002/1097-0290(20010105)72:1<85::AID-BIT12>3.0.CO
[38]  
2-H
[39]   PRODUCTION OF ABNORMAL PROTEINS IN ESCHERICHIA-COLI STIMULATES TRANSCRIPTION OF ION AND OTHER HEAT-SHOCK GENES [J].
GOFF, SA ;
GOLDBERG, AL .
CELL, 1985, 41 (02) :587-595
[40]   Sequential mechanism of solubilization and refolding of stable protein aggregates by a bichaperone network [J].
Goloubinoff, P ;
Mogk, A ;
Ben Zvi, AP ;
Tomoyasu, T ;
Bukau, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :13732-13737