The Mitochondrial Permeability Transition Pore: Past, Present, and Future.

IF 12.9 1区 生物学 Q1 BIOPHYSICS
Annual Review of Biophysics Pub Date : 2026-05-01 Epub Date: 2025-12-12 DOI:10.1146/annurev-biophys-030722-020832
Michela Carraro, Christoph Gerle, Paolo Bernardi
{"title":"The Mitochondrial Permeability Transition Pore: Past, Present, and Future.","authors":"Michela Carraro, Christoph Gerle, Paolo Bernardi","doi":"10.1146/annurev-biophys-030722-020832","DOIUrl":null,"url":null,"abstract":"<p><p>The mitochondrial permeability transition (PT) is a Ca2+-dependent permeability increase of the inner mitochondrial membrane mediated by opening of a high-conductance channel, the PT pore. Its molecular nature has been the subject of intense research and the source of controversies, but a considerable consensus has been reached that the PT originates from specific conformations of the F<sub>O</sub>F<sub>1</sub>-ATP synthase and of the adenine nucleotide translocator. The ATP synthase forms high-conductance channels in mammals and yeast but not in the anoxia- and salt-tolerant brine shrimp <i>Artemia franciscana</i>, which is refractory to the PT; it forms low-conductance and Ca2+-selective channels in <i>Drosophila melanogaster</i>, which undergoes a process of Ca2+-induced Ca2+ release but not a PT. The structural definition of ATP synthases from several species may allow for some inferences to be made about the mechanism of channel formation, or lack thereof, and provides a testable framework for future research.</p>","PeriodicalId":50756,"journal":{"name":"Annual Review of Biophysics","volume":" ","pages":"93-112"},"PeriodicalIF":12.9000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual Review of Biophysics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1146/annurev-biophys-030722-020832","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

The mitochondrial permeability transition (PT) is a Ca2+-dependent permeability increase of the inner mitochondrial membrane mediated by opening of a high-conductance channel, the PT pore. Its molecular nature has been the subject of intense research and the source of controversies, but a considerable consensus has been reached that the PT originates from specific conformations of the FOF1-ATP synthase and of the adenine nucleotide translocator. The ATP synthase forms high-conductance channels in mammals and yeast but not in the anoxia- and salt-tolerant brine shrimp Artemia franciscana, which is refractory to the PT; it forms low-conductance and Ca2+-selective channels in Drosophila melanogaster, which undergoes a process of Ca2+-induced Ca2+ release but not a PT. The structural definition of ATP synthases from several species may allow for some inferences to be made about the mechanism of channel formation, or lack thereof, and provides a testable framework for future research.

线粒体通透性过渡孔:过去,现在和未来。
线粒体通透性转变(PT)是Ca2+依赖的线粒体内膜通透性增加,通过打开一个高电导通道,即PT孔介导。其分子性质一直是激烈研究的主题和争议的来源,但已经达成了相当大的共识,即PT起源于FOF1-ATP合成酶和腺嘌呤核苷酸转运子的特定构象。ATP合酶在哺乳动物和酵母中形成高导通道,但在耐缺氧和耐盐的卤虾(Artemia franciscana)中不形成高导通道。它在果蝇中形成低电导和Ca2+选择性通道,经历Ca2+诱导的Ca2+释放过程,而不是PT。来自几个物种的ATP合酶的结构定义可能允许一些关于通道形成机制的推断,或缺乏它,并为未来的研究提供一个可测试的框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Annual Review of Biophysics
Annual Review of Biophysics 生物-生物物理
CiteScore
21.00
自引率
0.00%
发文量
25
期刊介绍: The Annual Review of Biophysics, in publication since 1972, covers significant developments in the field of biophysics, including macromolecular structure, function and dynamics, theoretical and computational biophysics, molecular biophysics of the cell, physical systems biology, membrane biophysics, biotechnology, nanotechnology, and emerging techniques.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书