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ProteomicsListeria monocytogenes exploits the MICOS complex subunit Mic10 to promote mitochondrial fragmentation and cellular infection
Mitochondrial function adapts to cellular demands and is affected by the ability of the organelle to undergo fusion and fission in response to physiological and non-physiological cues. We previously showed that infection with the human bacterial pathogen Listeria monocytogenes elicits transient mito...
ORGANISM(S): Homo sapiens (Human) 
2020-02-17 | PXD014667 | Pride
Micos complex Human Listeria monocytogenes Mitochondria Mic10 
UnknownDual role of Mic10 in mitochondrial cristae organization and ATP synthase-linked metabolic adaptation and respiratory growth.
Not available
S-EPMC8810396 | biostudies-literature
UnknownListeria monocytogenes Exploits Mitochondrial Contact Site and Cristae Organizing System Complex Subunit Mic10 To Promote Mitochondrial Fragmentation and Cellular Infection.
Not available
S-EPMC7002346 | biostudies-literature
UnknownCristae architecture is determined by an interplay of the MICOS complex and the F1FO ATP synthase via Mic27 and Mic10.
Not available
S-EPMC5568431 | biostudies-literature
UnknownSLP2 and MIC13 synergistically coordinate MICOS assembly and crista junction formation.
Not available
S-EPMC11667180 | biostudies-literature
UnknownDrosophila MIC10b can polymerize into cristae-shaping filaments.
Not available
S-EPMC10803214 | biostudies-literature
UnknownCHCHD2 maintains mitochondrial contact site and cristae organizing system stability and protects against mitochondrial dysfunction in an experimental model of Parkinson's disease.
Not available
S-EPMC9532036 | biostudies-literature
UnknownImbalance in MICOS Proteins in Rat Liver Mitochondria in an Induced Hyperthyroidism Model.
Not available
S-EPMC12691126 | biostudies-literature
ProteomicsMICOS and F1FO-ATP synthase crosstalk is a fundamental property of mitochondrial cristae
Mitochondrial cristae are polymorphic invaginations of the inner membrane that are the fabric of cellular respiration. Both the Mitochondrial Contact Site and Cristae Organization System (MICOS) and the F1FO-ATP synthase are vital for sculpting cristae by opposing membrane bending forces. While MICO...
ORGANISM(S): Trypanosoma brucei brucei TREU927 
2021-06-15 | PXD025109 | Pride
Micos Ip Lc-ms 
UnknownMulticolor 3D MINFLUX nanoscopy of mitochondrial MICOS proteins.
Not available
S-EPMC7456099 | biostudies-literature
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