Proteomics

Dataset Information

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Purified Porcine ATP synthaseLCMSMS


ABSTRACT: Purified mitochondrial ATP synthase has been shown to form Ca2+-activated, large conductance channel activity similar to that of mitochondrial megachannel (MMC) or mitochondrial permeability transition pore (mPTP) but the oligomeric state required for channel formation is being debated. We reconstitute purified monomeric ATP synthase from porcine heart mitochondria into small unilamellar vesicles (SUVs) with the lipid composition of mitochondrial inner membrane and analyze its oligomeric state by electron cryomicroscopy. The cryo-EM density map reveals the presence of a single ATP synthase monomer with no density seen for a second molecule tilted at an 86o angle relative to the first. We show that this preparation of SUV-reconstituted ATP synthase monomers, when fused into giant unilamellar vesicles (GUVs), forms voltage-gated and Ca2+-activated channels with the key features of mPTP. Based on our findings we conclude that the ATP synthase monomer is sufficient, and dimer formation is not required, for mPTP activity.

INSTRUMENT(S): Orbitrap Fusion

ORGANISM(S): Sus Scrofa Domesticus (domestic Pig)

TISSUE(S): Heart

SUBMITTER: Nelli Mnatsakanyan  

LAB HEAD: Elizabeth Jonas

PROVIDER: PXD016255 | Pride | 2020-01-13

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
ATPsynthase_MS.sf3 Other
OTF18-0985_Nelli_ATPsynthase_DDA_Sample2_Chymo.raw2.byspec2 Raw
OTF18-0985_Nelli_ATPsynthase_DDA_Sample2_Chymo2.raw Raw
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Publications

A mitochondrial megachannel resides in monomeric F<sub>1</sub>F<sub>O</sub> ATP synthase.

Mnatsakanyan Nelli N   Llaguno Marc C MC   Yang Youshan Y   Yan Yangyang Y   Weber Joachim J   Sigworth Fred J FJ   Jonas Elizabeth A EA  

Nature communications 20191220 1


Purified mitochondrial ATP synthase has been shown to form Ca<sup>2+</sup>-activated, large conductance channel activity similar to that of mitochondrial megachannel (MMC) or mitochondrial permeability transition pore (mPTP) but the oligomeric state required for channel formation is being debated. We reconstitute purified monomeric ATP synthase from porcine heart mitochondria into small unilamellar vesicles (SUVs) with the lipid composition of mitochondrial inner membrane and analyze its oligome  ...[more]

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