Acta Biochimica et Biophysica Sinica · 2004 · 20 citations · 10 references
Life SciencesBiologyMolecular BiologyEnzymologyGene ExpressionMicrobial GeneticsEnzyme ExpressionEnzyme FunctionHeterologous Protein ExpressionCloningEscherichia ColiMolecular Cloning ApplicationsOpen Reading Frame IdentificationOpen Reading Frame LengthRefolding Of Inclusion BodiesSecreted Proteases
The earthworm fibrinolytic enzyme-3 (EFE-3, GenBank accession No: AY438622), from the earthworm Eisenia foetida, is a component of earthworm fibrinolytic enzymes. In this study, cDNA encoding the EFE-3 was cloned by RT-PCR. The cDNA contained an open reading frame of 741 nucleotides, which encoded a deduced protein of 247 amino acid residues, including signal sequences. EFE-3 showed a high degree of homology to earthworm (Lumbricus rebullus) proteases F-III-1, F-III-2, and bovine trypsin. The recombinant EFE-3 was expressed in E. coli as inclusion bodies, and the gene encoding the native form of EFE-3 was expressed in COS-7 cells in the medium. Both the refolding product of inclusion bodies and the secreted protease could dissolve the artificial fibrin plate.
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In vitro folding of inclusion body proteins
Rainer Rudolph, Hauke Lilie · The FASEB Journal · 1996 · 662 citations