Jensen T G, Bross P, Andresen B S, Lund T B, Kristensen T J, Jensen U B, Winther V, Kølvraa S, Gregersen N, Bolund L
Institute of Human Genetics, University of Aarhus, Denmark.
Hum Mutat. 1995;6(3):226-31. doi: 10.1002/humu.1380060305.
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially lethal inherited defect in the beta-oxidation of fatty acids. By comparing the behaviour of five missense MCAD mutant proteins expressed in COS cells and in Escherichia coli, we can define some of these as "pure folding mutants." Upon expression in E. coli, these mutant proteins produce activity levels in the range of the wild-type enzyme only if the chaperonins GroESL are co-overproduced. When overexpressed in COS cells, the pure folding mutants display enzyme activities comparable to the wild-type enzyme. The results suggest that the MCAD mutations can be modulated by chaperones, a phenomenon that may influence the manifestation of the MCAD disease.
