| Literature DB >> 33402698 |
Alexander Mühleip1,2, Rasmus Kock Flygaard1,2, Jana Ovciarikova3, Alice Lacombe3, Paula Fernandes1,2,3, Lilach Sheiner4, Alexey Amunts5,6.
Abstract
Mitochondrial ATP synthase plays a key role in inducing membrane curvature to establish cristae. In Apicomplexa causing diseases such as malaria and toxoplasmosis, an unusual cristae morphology has been observed, but its structural basis is unknown. Here, we report that the apicomplexan ATP synthase assembles into cyclic hexamers, essential to shape their distinct cristae. Cryo-EM was used to determine the structure of the hexamer, which is held together by interactions between parasite-specific subunits in the lumenal region. Overall, we identified 17 apicomplexan-specific subunits, and a minimal and nuclear-encoded subunit-a. The hexamer consists of three dimers with an extensive dimer interface that includes bound cardiolipins and the inhibitor IF1. Cryo-ET and subtomogram averaging revealed that hexamers arrange into ~20-megadalton pentagonal pyramids in the curved apical membrane regions. Knockout of the linker protein ATPTG11 resulted in the loss of pentagonal pyramids with concomitant aberrantly shaped cristae. Together, this demonstrates that the unique macromolecular arrangement is critical for the maintenance of cristae morphology in Apicomplexa.Entities:
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Year: 2021 PMID: 33402698 PMCID: PMC7785744 DOI: 10.1038/s41467-020-20381-z
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919