{"title":"提高质子与ATP比值的ATP合酶工程","authors":"Hiroshi Ueno, Kiyoto Yasuda, Norie Hamaguchi-Suzuki, Riku Marui, Naruhiko Adachi, Toshiya Senda, Takeshi Murata, Hiroyuki Noji","doi":"10.1038/s41467-025-61227-w","DOIUrl":null,"url":null,"abstract":"<p>F<sub>o</sub>F<sub>1</sub>-ATP synthase (F<sub>o</sub>F<sub>1</sub>) interconverts the energy of the proton motive force (<i>pmf</i>) and that of ATP through the mechanical rotation. The H<sup>+</sup>/ATP ratio, one of the most crucial parameters in bioenergetics, varies among species due to differences in the number of H<sup>+</sup>-binding c-subunits, resulting in H<sup>+</sup>/ATP ratios ranging from 2.7 to 5. In this study, we seek to significantly enhance the H<sup>+</sup>/ATP ratio by employing an alternative approach that differs from that of nature. We engineer F<sub>o</sub>F<sub>1</sub> to form multiple peripheral stalks, each bound to a proton-conducting a-subunit. The engineered F<sub>o</sub>F<sub>1</sub> exhibits an H<sup>+</sup>/ATP ratio of 5.8, surpassing the highest ratios found in naturally occurring F<sub>o</sub>F<sub>1</sub>s, enabling ATP synthesis under low <i>pmf</i> conditions where wild-type enzymes cannot synthesize ATP. Structural analysis reveals that the engineered F<sub>o</sub>F<sub>1</sub> forms up to three peripheral stalks and a-subunits. This study not only provides valuable insights into the H<sup>+</sup>-transport mechanism of F<sub>o</sub>F<sub>1</sub> but also opens up possibilities for engineering the foundation of cellular bioenergetics.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"48 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Engineering of ATP synthase for enhancement of proton-to-ATP ratio\",\"authors\":\"Hiroshi Ueno, Kiyoto Yasuda, Norie Hamaguchi-Suzuki, Riku Marui, Naruhiko Adachi, Toshiya Senda, Takeshi Murata, Hiroyuki Noji\",\"doi\":\"10.1038/s41467-025-61227-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>F<sub>o</sub>F<sub>1</sub>-ATP synthase (F<sub>o</sub>F<sub>1</sub>) interconverts the energy of the proton motive force (<i>pmf</i>) and that of ATP through the mechanical rotation. The H<sup>+</sup>/ATP ratio, one of the most crucial parameters in bioenergetics, varies among species due to differences in the number of H<sup>+</sup>-binding c-subunits, resulting in H<sup>+</sup>/ATP ratios ranging from 2.7 to 5. In this study, we seek to significantly enhance the H<sup>+</sup>/ATP ratio by employing an alternative approach that differs from that of nature. We engineer F<sub>o</sub>F<sub>1</sub> to form multiple peripheral stalks, each bound to a proton-conducting a-subunit. The engineered F<sub>o</sub>F<sub>1</sub> exhibits an H<sup>+</sup>/ATP ratio of 5.8, surpassing the highest ratios found in naturally occurring F<sub>o</sub>F<sub>1</sub>s, enabling ATP synthesis under low <i>pmf</i> conditions where wild-type enzymes cannot synthesize ATP. Structural analysis reveals that the engineered F<sub>o</sub>F<sub>1</sub> forms up to three peripheral stalks and a-subunits. This study not only provides valuable insights into the H<sup>+</sup>-transport mechanism of F<sub>o</sub>F<sub>1</sub> but also opens up possibilities for engineering the foundation of cellular bioenergetics.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"48 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-61227-w\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-61227-w","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Engineering of ATP synthase for enhancement of proton-to-ATP ratio
FoF1-ATP synthase (FoF1) interconverts the energy of the proton motive force (pmf) and that of ATP through the mechanical rotation. The H+/ATP ratio, one of the most crucial parameters in bioenergetics, varies among species due to differences in the number of H+-binding c-subunits, resulting in H+/ATP ratios ranging from 2.7 to 5. In this study, we seek to significantly enhance the H+/ATP ratio by employing an alternative approach that differs from that of nature. We engineer FoF1 to form multiple peripheral stalks, each bound to a proton-conducting a-subunit. The engineered FoF1 exhibits an H+/ATP ratio of 5.8, surpassing the highest ratios found in naturally occurring FoF1s, enabling ATP synthesis under low pmf conditions where wild-type enzymes cannot synthesize ATP. Structural analysis reveals that the engineered FoF1 forms up to three peripheral stalks and a-subunits. This study not only provides valuable insights into the H+-transport mechanism of FoF1 but also opens up possibilities for engineering the foundation of cellular bioenergetics.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.