Human F1F0 ATP synthase, mitochondrial ultrastructure and OXPHOS impairment: a (super-)complex matter?
Mitochondrial morphogenesis is a key process of cell physiology. It is essential for the proper function of this double membrane-delimited organelle, as it ensures the packing of the inner membrane in a very ordered pattern called cristae. In yeast, the mitochondrial ATP synthase is able to form dim...
Saved in:
Main Authors: | Johann Habersetzer, Isabelle Larrieu, Muriel Priault, Bénédicte Salin, Rodrigue Rossignol, Daniel Brèthes, Patrick Paumard |
---|---|
Format: | article |
Language: | EN |
Published: |
Public Library of Science (PLoS)
2013
|
Subjects: | |
Online Access: | https://doaj.org/article/ce38a0987d5049aeb3205867d93bbf07 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A mitochondrial megachannel resides in monomeric F1FO ATP synthase
by: Nelli Mnatsakanyan, et al.
Published: (2019) -
Deregulation of mitochondrial F1FO-ATP synthase via OSCP in Alzheimer’s disease
by: Simon J. Beck, et al.
Published: (2016) -
Defining the molecular mechanisms of the mitochondrial permeability transition through genetic manipulation of F-ATP synthase
by: Andrea Carrer, et al.
Published: (2021) -
Modulation and Pharmacology of the Mitochondrial Permeability Transition: A Journey from F-ATP Synthase to ANT
by: Andrea Carrer, et al.
Published: (2021) -
INA complex liaises the F1Fo-ATP synthase membrane motor modules
by: Nataliia Naumenko, et al.
Published: (2017)