AUTHOR=Haskins Nantaporn , Bhuvanendran Shivaprasad , Anselmi Claudio , Gams Anna , Kanholm Tomas , Kocher Kristen M. , LoTempio Jonathan , Krohmaly Kylie I. , Sohai Danielle , Stearrett Nathaniel , Bonner Erin , Tuchman Mendel , Morizono Hiroki , Jaiswal Jyoti K. , Caldovic Ljubica TITLE=Mitochondrial Enzymes of the Urea Cycle Cluster at the Inner Mitochondrial Membrane JOURNAL=Frontiers in Physiology VOLUME=11 YEAR=2021 URL=https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2020.542950 DOI=10.3389/fphys.2020.542950 ISSN=1664-042X ABSTRACT=
Mitochondrial enzymes involved in energy transformation are organized into multiprotein complexes that channel the reaction intermediates for efficient ATP production. Three of the mammalian urea cycle enzymes: N-acetylglutamate synthase (NAGS), carbamylphosphate synthetase 1 (CPS1), and ornithine transcarbamylase (OTC) reside in the mitochondria. Urea cycle is required to convert ammonia into urea and protect the brain from ammonia toxicity. Urea cycle intermediates are tightly channeled in and out of mitochondria, indicating that efficient activity of these enzymes relies upon their coordinated interaction with each other, perhaps in a cluster. This view is supported by mutations in surface residues of the urea cycle proteins that impair ureagenesis in the patients, but do not affect protein stability or catalytic activity. We find the NAGS, CPS1, and OTC proteins in liver mitochondria can associate with the inner mitochondrial membrane (IMM) and can be co-immunoprecipitated. Our