EXPRESSION AND COUPLING OF HUMAN CYTOCHROME-P450 2E1 AND NADPH-CYTOCHROME P450 OXIDOREDUCTASE IN DUAL EXPRESSION AND COINFECTION SYSTEMS WITH BACULOVIRUS IN INSECT CELLS
Mh. Wang et al., EXPRESSION AND COUPLING OF HUMAN CYTOCHROME-P450 2E1 AND NADPH-CYTOCHROME P450 OXIDOREDUCTASE IN DUAL EXPRESSION AND COINFECTION SYSTEMS WITH BACULOVIRUS IN INSECT CELLS, Archives of biochemistry and biophysics, 334(2), 1996, pp. 380-388
in order to study the interaction between human cytochrome P450 2E1 (h
2E1) and NADPH-P450 oxidoreductase (hOR) in a native membrane environm
ent, we used two approaches to express both h2E1 and hOR in a baculovi
rus expression system. For a dual-expression system, h2E1 and hOR were
coexpressed in Spodoptera frugiperda (Sf9) insect cells using a recom
binant baculovirus carrying both h2E1 and hOR cDNAs (v-h2E1-hOR). The
h2E1 cDNA was expressed under the control of the polyhedrin promoter P
-Polh, whereas hOR cDNA was expressed under the control of the P-10 pr
omoter. The expressed enzymes were catalytically active in the cell me
mbrane preparations. The estimated molar expression ratio of h2E1 to h
OR in the membranes was 1:5. The apparent K-m and k(cat) for N-nitroso
dimethylamine (NDMA) demethylase activity were 145 mu M and 2.4 min(-1
), respectively. When Sf9 cells were co-infected with the dual-express
ion virus (v-h2E1-hOR) and human cytochrome b(5) recombinant virus (v-
hb(5)), a 9-fold decrease in the K-m, of NDMA demethylase activity (16
mu M) was observed in the membrane preparations, whereas the k(cat) w
as increased to 4 min(-1). In the second approach, recombinant viruses
of h2E1 and hOR (v-h2E1 and v-hOR) were used to coinfect the Sf9 cell
s. in this double-expression system, with a fixed amount of v-h2E1, th
e expression of h2E1 in the Sf9 cells decreased as the amount of v-hOR
increased. Western blot analysis of the membrane preparations showed
that the level of hOR increased, but the level of h2E1 decreased with
increasing amounts of v-hOR. A corresponding decrease in h2E1 mRNA, ho
wever, was not observed. In the presence of human cytochrome b(5) (hb(
5)), the optimal h2E1:hOR molar ratio for h2E1 catalytic activity was
1:1. In order to further investigate the hb(5) effect on h2E1-catalyze
d reactions in the native membranes, we co-infected Sig cells with v-h
2E1, v-hOR, and v-hb(5) and obtained a membrane preparation containing
h2E1, hOR, and hbs. Stoichiometric analysis with membrane preparation
s from double-infection and triple-infection systems revealed that the
presence of hb(5) decreased NADPH oxidation and H2O2 formation by 72
and 80%, respectively, but increased product formation from NDMA. 13-f
old. These results suggest that hb(5) enhances the coupling between h2
E1 and hOR for product formation. These studies also demonstrate that
the baculovirus-insect cell system can produce high levels of expressi
on of functional h2E1, hOR, and hb(5) for mechanistic studies. (C) 199
6 Academic Press, Inc.