Membrane-Anchored Cyclic Peptides as Effectors of
Mitochondrial Oxidative Phosphorylation
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Version 1 2016-03-29, 15:03Version 1 2016-03-29, 15:03
Posted on 2016-03-17 - 00:00
The
echinocandins are membrane-anchored, cyclic lipopeptides (CLPs)
with antifungal activity due to their ability to inhibit a glucan
synthase located in the plasma membrane of fungi such as Candida
albicans. A hydrophobic tail of an echinocandin CLP inserts
into a membrane, placing a six-amino acid cyclic peptide near the
membrane surface. Because processes critical for the function of the
electron transfer complexes of mitochondria, such as proton uptake
and release, take place near the surface of the membrane, we have
tested the ability of two echinocandin CLPs, caspofungin and micafungin,
to affect the activity of electron transfer complexes in isolated
mammalian mitochondria. Indeed, caspofungin and micafungin both inhibit
whole chain electron transfer in isolated mitochondria at low micromolar
concentrations. The effects of the CLPs are fully reversible, in some
cases simply via the addition of bovine serum albumin to bind the
CLPs via their hydrophobic tails. Each CLP affects more than one complex,
but they still exhibit specificity of action. Only caspofungin inhibits
complex I, and the CLP inhibits liver but not heart complex I. Both
CLPs inhibit heart and liver complex III. Caspofungin inhibits complex
IV activity, while, remarkably, micafungin stimulates complex IV activity
nearly 3-fold. Using a variety of assays, we have developed initial
hypotheses for the mechanisms by which caspofungin and micafungin
alter the activities of complexes IV and III. The dication caspofungin
partially inhibits cytochrome c binding at the low-affinity
binding site of complex IV, while it also appears to inhibit the release
of protons from the outer surface of the complex, similar to Zn2+. Anionic micafungin appears to stimulate complex IV activity
by enhancing the transfer of protons to the O2 reduction
site. For complex III, we hypothesize that each CLP binds to the cytochrome b subunit and the Fe–S subunit to inhibit the required
rotational movement of the latter.
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Shirey, Kristin; Stover, Kayla
R.; Cleary, John; Hoang, Ngoc; Hosler, Jonathan (2016). Membrane-Anchored Cyclic Peptides as Effectors of
Mitochondrial Oxidative Phosphorylation. ACS Publications. Collection. https://doi.org/10.1021/acs.biochem.5b01368