PMID- 23405277 OWN - NLM STAT- MEDLINE DCOM- 20130819 LR - 20220223 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 3 DP - 2013 TI - Identification of cardiolipin binding sites on cytochrome c oxidase at the entrance of proton channels. PG - 1263 LID - 10.1038/srep01263 [doi] LID - 1263 AB - The respiratory chain or oxidative phosphorylation system (OxPhos) generates most of the chemical energy (ATP) used by our cells. The cytochrome c oxidase (CcO) is one of three protein complexes of OxPhos building up a proton gradient across the inner mitochondrial membrane, which is ultimately used by the ATP synthase to produce ATP. We present molecular dynamic simulations of CcO in a mimic of the mitochondrial membrane, and identify precise binding sites of cardiolipin (CL, signature phospholipid of mitochondria) on the protein surface. Two of these CL binding sites reveal pathways linking CLs to the entrance of the D and H proton channels across CcO. CLs being able to carry protons our results strongly support an involvement of CLs in the proton delivery machinery to CcO. The ubiquitous nature of CL interactions with the components of the OxPhos suggests that this delivery mechanism might extend to the other respiratory complexes. FAU - Arnarez, C AU - Arnarez C AD - Groningen Biomolecular Sciences and Biotechnology Institute and Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands. FAU - Marrink, S J AU - Marrink SJ FAU - Periole, X AU - Periole X LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130212 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Cardiolipins) RN - 0 (Lipids) RN - 0 (Protons) RN - EC 1.9.3.1 (Electron Transport Complex IV) SB - IM EIN - Sci Rep. 2013;3:1343 MH - Animals MH - Binding Sites MH - Cardiolipins/chemistry/*metabolism MH - Cattle MH - Crystallography, X-Ray MH - Electron Transport Complex IV/chemistry/*metabolism MH - Hydrogen Bonding MH - Lipids/chemistry MH - Molecular Docking Simulation MH - Protein Structure, Tertiary MH - Protons PMC - PMC3570132 EDAT- 2013/02/14 06:00 MHDA- 2013/08/21 06:00 PMCR- 2013/02/12 CRDT- 2013/02/14 06:00 PHST- 2012/11/20 00:00 [received] PHST- 2013/01/07 00:00 [accepted] PHST- 2013/02/14 06:00 [entrez] PHST- 2013/02/14 06:00 [pubmed] PHST- 2013/08/21 06:00 [medline] PHST- 2013/02/12 00:00 [pmc-release] AID - srep01263 [pii] AID - 10.1038/srep01263 [doi] PST - ppublish SO - Sci Rep. 2013;3:1263. doi: 10.1038/srep01263. Epub 2013 Feb 12.