{"title":"膜曲率控制氧化磷酸化系统的效率","authors":"S. V. Nesterov","doi":"10.1134/S1990747825700059","DOIUrl":null,"url":null,"abstract":"<p>This paper analyzes the structural and functional organization of mitochondria. It is shown that deformation of membrane lipids by supercomplexes of the mitochondrial respiratory chain and ATP synthase dimers leads to their mutual attraction. It has been shown that membrane bending near the proton pump creates a dedicated direction for the movement of protons to ATP synthase. Mitochondria can operate in the standby mode with loose coupling but also with low oxidative damage. They can switch to the mode of tight coupling and clustering of oxidative phosphorylation system (OXPHOS) at high energy demand conditions due to the changes in ultrastructure.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"19 Proceedings","pages":"151 - 156"},"PeriodicalIF":1.4000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Membrane Curvature Controls the Efficiency of Oxidative Phosphorylation System\",\"authors\":\"S. V. Nesterov\",\"doi\":\"10.1134/S1990747825700059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This paper analyzes the structural and functional organization of mitochondria. It is shown that deformation of membrane lipids by supercomplexes of the mitochondrial respiratory chain and ATP synthase dimers leads to their mutual attraction. It has been shown that membrane bending near the proton pump creates a dedicated direction for the movement of protons to ATP synthase. Mitochondria can operate in the standby mode with loose coupling but also with low oxidative damage. They can switch to the mode of tight coupling and clustering of oxidative phosphorylation system (OXPHOS) at high energy demand conditions due to the changes in ultrastructure.</p>\",\"PeriodicalId\":484,\"journal\":{\"name\":\"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology\",\"volume\":\"19 Proceedings\",\"pages\":\"151 - 156\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1990747825700059\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","FirstCategoryId":"2","ListUrlMain":"https://link.springer.com/article/10.1134/S1990747825700059","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Membrane Curvature Controls the Efficiency of Oxidative Phosphorylation System
This paper analyzes the structural and functional organization of mitochondria. It is shown that deformation of membrane lipids by supercomplexes of the mitochondrial respiratory chain and ATP synthase dimers leads to their mutual attraction. It has been shown that membrane bending near the proton pump creates a dedicated direction for the movement of protons to ATP synthase. Mitochondria can operate in the standby mode with loose coupling but also with low oxidative damage. They can switch to the mode of tight coupling and clustering of oxidative phosphorylation system (OXPHOS) at high energy demand conditions due to the changes in ultrastructure.
期刊介绍:
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology is an international peer reviewed journal that publishes original articles on physical, chemical, and molecular mechanisms that underlie basic properties of biological membranes and mediate membrane-related cellular functions. The primary topics of the journal are membrane structure, mechanisms of membrane transport, bioenergetics and photobiology, intracellular signaling as well as membrane aspects of cell biology, immunology, and medicine. The journal is multidisciplinary and gives preference to those articles that employ a variety of experimental approaches, basically in biophysics but also in biochemistry, cytology, and molecular biology. The journal publishes articles that strive for unveiling membrane and cellular functions through innovative theoretical models and computer simulations.