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Assembly and functional expression of murine glutathione reductase cDNA: a sequence missing in expressed sequence tag
R Iozef1, K Becker, C C Boehme
1Center of Biochemistry, Heidelberg University, Im Neuenheimer Feld 328, D-69120, Heidelberg, Germany.
Biochimica Et Biophysica Acta
|November 24, 1999
Abstract:
Glutathione reductase (GR) is a chemotherapeutic target. Murine GRcDNA, which contains 85% GC in the 38 codons following the start codon, was assembled from the PCR-amplified exon 1 and a downstream cDNA prior to expression in Escherichia coli as a His(6)-tagged protein. Recombinant GR, an FAD-containing homodimer, corresponds in its enzymic and spectral properties to GR isolated from murine Ehrlich ascites tumor cells. Another cDNA, representing GR with a mitochondrial targeting sequence, yielded two distinct enzymically active expression products.