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J. Biol. Chem., Vol. 263, Issue 33, 17422-17428, Nov, 1988
KK Arora and PL Pedersen
Previous studies from this laboratory have shown that mitochondrial bound
hexokinase is markedly elevated in highly glycolytic hepatoma cells (Parry,
D. M., and Pedersen, P.L. (1983) J. Biol. Chem. 258, 10904-10912). A
pore-forming protein, porin, within the outer membrane appears to comprise
at least part of the receptor site (Nakashima, R.A., Mangan, P.S.,
Colombini, M., and Pedersen, P.L. (1986). Biochemistry 25, 1015-1021). In
studies reported here experiments were carried out to assess the functional
significance of mitochondrial bound tumor hexokinase. Two approaches were
used to determine whether the bound enzyme has preferred access to
mitochondrially generated ATP relative to cytosolic ATP. The first approach
compared the time course of glucose 6-phosphate formation by AS-30D
hepatoma mitochondria under conditions where ATP was regenerated
endogenously via oxidative phosphorylation or exogenously by added pyruvate
kinase and phosphoenolpyruvate. The second approach involved the
measurement of the specific radioactivity of glucose 6-phosphate formed
following the addition of [gamma-32P]ATP to either phosphorylating or
nonphosphorylating AS-30D mitochondria. Both approaches provided results
which show that the source of ATP for bound hexokinase is derived
preferentially from the ATP synthase residing within the inner
mitochondrial membrane compartment rather than from the medium (i.e. from
the cytosolic compartment). These results provide the first direct
demonstration that the exceptionally high level of hexokinase bound to
mitochondria of highly glycolytic tumor cells has preferred access to
mitochondrially generated ATP, a finding that may have rather profound
metabolic significance for such tumors.
Functional significance of mitochondrial bound hexokinase in tumor cell metabolism. Evidence for preferential phosphorylation of glucose by intramitochondrially generated ATP
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
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