Amyloids in bacterial inclusion bodies

被引:105
作者
de Groot, Natalia S.
Sabate, Raimon
Ventura, Salvador [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Bioquim & Biol Mol, E-08193 Barcelona, Spain
关键词
PROTEIN AGGREGATION; THERMODYNAMIC STABILITY; GLOBULAR-PROTEINS; ESCHERICHIA-COLI; IN-VIVO; MOLECULAR-MECHANISMS; RECOMBINANT PROTEINS; SPECIFICITY; EXPRESSION; MUTATIONS;
D O I
10.1016/j.tibs.2009.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Protein misfolding and aggregation into amyloid structures are associated with dozens of human diseases. Recent studies have provided compelling evidence for the existence of highly ordered, amyloid-like conformations in the insoluble inclusion bodies produced during heterologous protein expression in bacteria. Thus, amyloid aggregation seems to be an omnipresent process in both eukaryotic and prokaryotic organisms. Amyloid formation inside cell factories raises important safety concerns with regard to the toxicity and infectivity of recombinant proteins. Yet such findings also suggest that prokaryotic cells could be useful systems for studying how and why proteins aggregate in vivo, and they could also provide a biologically relevant background for screening therapeutic approaches to pathologic protein deposition.
引用
收藏
页码:408 / 416
页数:9
相关论文
共 75 条
[1]
Kinetics of inclusion body formation studied in intact cells by FT-IR spectroscopy [J].
Ami, D ;
Natalello, A ;
Gatti-Lafranconi, P ;
Lotti, M ;
Doglia, SM .
FEBS LETTERS, 2005, 579 (16) :3433-3436
[2]
Effects of recombinant protein misfolding and aggregation on bacterial membranes [J].
Ami, D. ;
Natalello, A. ;
Schultz, T. ;
Gatti-Lafnanconi, P. ;
Lotti, M. ;
Doglia, S. M. ;
de Marco, A. .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2009, 1794 (02) :263-269
[3]
Domain organization and structure-function relationship of the HET-s prion protein of Podospora anserina [J].
Balguerie, A ;
Dos Reis, S ;
Ritter, C ;
Chaignepain, S ;
Coulary-Salin, B ;
Forge, V ;
Bathany, K ;
Lascu, I ;
Schmitter, JM ;
Riek, R ;
Saupe, SJ .
EMBO JOURNAL, 2003, 22 (09) :2071-2081
[4]
Delineating common molecular mechanisms in Alzheimer's and prion diseases [J].
Barnham, Kevin J. ;
Cappai, Roberto ;
Beyreuther, Konrad ;
Masters, Colin L. ;
Hill, Andrew F. .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (08) :465-472
[5]
STRUCTURE AND MORPHOLOGY OF PROTEIN INCLUSION-BODIES IN ESCHERICHIA-COLI [J].
BOWDEN, GA ;
PAREDES, AM ;
GEORGIOU, G .
BIO-TECHNOLOGY, 1991, 9 (08) :725-730
[6]
Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases [J].
Bucciantini, M ;
Giannoni, E ;
Chiti, F ;
Baroni, F ;
Formigli, L ;
Zurdo, JS ;
Taddei, N ;
Ramponi, G ;
Dobson, CM ;
Stefani, M .
NATURE, 2002, 416 (6880) :507-511
[7]
Investigating the effects of mutations on protein aggregation in the cell [J].
Calloni, G ;
Zoffoli, S ;
Stefani, M ;
Dobson, CM ;
Chiti, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (11) :10607-10613
[8]
Local cooperativity in the unfolding of an amyloidogenic variant of human lysozyme [J].
Canet, D ;
Last, AM ;
Tito, P ;
Sunde, M ;
Spencer, A ;
Archer, DB ;
Redfield, C ;
Robinson, CV ;
Dobson, CM .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (04) :308-315
[9]
Amyloid-like properties of bacterial inclusion bodies [J].
Carrió, M ;
González-Montalbán, N ;
Vera, A ;
Villaverde, A ;
Ventura, S .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 347 (05) :1025-1037
[10]
Localization of chaperones DnaK and GroEL in bacterial inclusion bodies [J].
Carrió, MM ;
Villaverde, A .
JOURNAL OF BACTERIOLOGY, 2005, 187 (10) :3599-3601