Coproduction of DnaK/DnaJ in Escherichia coli enhances solubility but promotes proteolytic degradation of their substrates, minimizing the yield of unstable polypeptides. Higher eukaryotes have orthologs of DnaK/DnaJ but lack the linked bacterial proteolytic system. By coexpression of DnaK and DnaJ in insect cells with inherently misfolding-prone recombinant proteins, we demonstrate simultaneous improvement of soluble protein yield and quality and proteolytic stability. Thus, undesired side effects of bacterial folding modulators can be avoided by appropriate rehosting in heterologous cell expression systems
AbstractA role for DnaK, the major E. coli Hsp70, in chaperoning de novo protein folding has remaine...
The physiological consequences of molecular chaperone overproduction in Escherichia coli are present...
Despite the fundamental importance of E. coli in the manufacture of a wide range of biotechnological...
Coproduction of DnaK/DnaJ in Escherichia coli enhances solubility but promotes proteolytic degradati...
The DnaK/DnaJ Escherichia coli chaperone pair, co-produced along with recombinant proteins, has been...
Main Escherichia coli cytosolic chaperones such as DnaK are key components of the control quality ne...
Misfolding-prone proteins produced in bacteria usually fail to adopt their native conformation and a...
Background: The overproduction of recombinant proteins in host cells often leads to their misfolding...
Abstract Background The overproduction of recombinant proteins in host cells often leads to their mi...
Abstract Insufficient availability of molecular chaperones is observed as a major bottleneck for pro...
AbstractTrigger factor and DnaK protect nascent protein chains from misfolding and aggregation in th...
Recent evidence supports the view that cellular protein folding may be mediated by molecular chapero...
The recombinant expression of eukaryotic proteins in Escherichia coli often results in protein aggre...
Insufficient availability of molecular chaperones is observed as a major bottleneck for proper prote...
<div><p>Protein chaperones are essential in all domains of life to prevent and resolve protein misfo...
AbstractA role for DnaK, the major E. coli Hsp70, in chaperoning de novo protein folding has remaine...
The physiological consequences of molecular chaperone overproduction in Escherichia coli are present...
Despite the fundamental importance of E. coli in the manufacture of a wide range of biotechnological...
Coproduction of DnaK/DnaJ in Escherichia coli enhances solubility but promotes proteolytic degradati...
The DnaK/DnaJ Escherichia coli chaperone pair, co-produced along with recombinant proteins, has been...
Main Escherichia coli cytosolic chaperones such as DnaK are key components of the control quality ne...
Misfolding-prone proteins produced in bacteria usually fail to adopt their native conformation and a...
Background: The overproduction of recombinant proteins in host cells often leads to their misfolding...
Abstract Background The overproduction of recombinant proteins in host cells often leads to their mi...
Abstract Insufficient availability of molecular chaperones is observed as a major bottleneck for pro...
AbstractTrigger factor and DnaK protect nascent protein chains from misfolding and aggregation in th...
Recent evidence supports the view that cellular protein folding may be mediated by molecular chapero...
The recombinant expression of eukaryotic proteins in Escherichia coli often results in protein aggre...
Insufficient availability of molecular chaperones is observed as a major bottleneck for proper prote...
<div><p>Protein chaperones are essential in all domains of life to prevent and resolve protein misfo...
AbstractA role for DnaK, the major E. coli Hsp70, in chaperoning de novo protein folding has remaine...
The physiological consequences of molecular chaperone overproduction in Escherichia coli are present...
Despite the fundamental importance of E. coli in the manufacture of a wide range of biotechnological...