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South Bend Center for Medical Education, Indiana University School of Medicine, University of Notre Dame, Notre Dame, Indiana 46556
In
previous work (McKee EE, Bentley AT, Smith RM Jr, and Ciaccio CE,
Biochem Biophys Res Commun 257: 466-472, 1999), the transport of guanine nucleotides into the matrix of intact isolated heart mitochondria was demonstrated. In this study, the time course and
mechanisms of guanine nucleotide transport are characterized. Two
distinct mechanisms of transport were found to be capable of moving
guanine nucleotides across the inner membrane. The first carrier was
saturable, displayed temperature dependence, preferred GDP to GTP, and
did not transport GMP or IMP. When incubated in the absence of
exogenous ATP, this carrier had a Vmax of
946 ± 53 pmol · mg
1 · min
1 with a
Km of 2.9 ± 0.3 mM for GDP. However,
transport of GTP and GDP on this carrier was completely inhibited by
physiological concentrations of ATP, suggesting that this carrier was
not involved with guanine nucleotide transport in vivo. Because
transport on this carrier was also inhibited by atractyloside, this
carrier was consistent with the well-characterized ATP/ADP translocase. The second mechanism of guanine nucleotide uptake was insensitive to
atractyloside, displayed temperature dependence, and was capable of
transporting GMP, GDP, and GTP at approximately equal rates but did not
transport IMP, guanine, or guanosine. GTP transport via this mechanism
was slow, with a Vmax of 48.7 ± 1.4 pmol · mg
1 · min
1 and a
Km = 4.4 ± 0.4 mM. However, because
the requirement for guanine nucleotide transport is low in nondividing
tissues such as the heart, this transport process is nevertheless
sufficient to account for the matrix uptake of guanine nucleotides and
may represent the physiological mechanism of transport.
bioenergetics; nucleotide metabolism; biogenesis
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