首页> 外文期刊>Progress in Biophysics and Molecular Biology: An International Review Journal >Acidic lipids, H(+)-ATPases, and mechanism of oxidative phosphorylation. Physico-chemical ideas 30 years after P. Mitchell's Nobel Prize award
【24h】

Acidic lipids, H(+)-ATPases, and mechanism of oxidative phosphorylation. Physico-chemical ideas 30 years after P. Mitchell's Nobel Prize award

机译:酸性脂质,H(+)-ATPases和氧化磷酸化的机制。理查德·米切尔(P. Mitchell)获得诺贝尔奖30年后的理化思想

获取原文
获取原文并翻译 | 示例
           

摘要

Peter D. Mitchell, who was awarded the Nobel Prize in Chemistry 30 years ago, in 1978, formulated the chemiosmotic theory of oxidative phosphorylation. This review initially analyzes the major aspects of this theory, its unresolved problems, and its modifications. A new physico-chemical mechanism of energy transformation and coupling of oxidation and phosphorylation is then suggested based on recent concepts regarding proteins, including ATPases that work as molecular motors, and acidic lipids that act as hydrogen ion (H(+)) carriers. According to this proposed mechanism, the chemical energy of a redox substrate is transformed into nonequilibrium states of electron-transporting chain (ETC) coupling proteins. This leads to nonequilibrium pumping of H(+) into the membrane. An acidic lipid, cardiolipin, binds with this H(+) and carries it to the ATP-synthase along the membrane surface. This transport generates gradients of surface tension or electric field along the membrane surface. Hydrodynamic effects on a nanolevel lead to rotation of ATP-synthase and finally to the release of ATP into aqueous solution. This model also explains the generation of a transmembrane protonmotive force that is used for regulation of transmembrane transport, but is not necessary for the coupling of electron transport and ATP synthesis.
机译:彼得·D·米切尔(Peter D. Mitchell)于1978年获得30年前的诺贝尔化学奖,他提出了氧化磷酸化的化学渗透理论。本文首先对这一理论的主要方面,其未解决的问题及其修改进行了分析。然后,基于有关蛋白质的最新概念,提出了一种新的物理化学机制,涉及能量转换以及氧化和磷酸化的偶联,包括充当分子马达的ATPase和充当氢离子(H(+))载体的酸性脂质。根据此提出的机制,氧化还原底物的化学能被转换成电子传输链(ETC)偶联蛋白的非平衡态。这导致将H(+)非平衡泵送到膜中。酸性脂质心磷脂与该H(+)结合并沿着膜表面将其携带到ATP合酶。这种传输沿膜表面产生表面张力或电场的梯度。纳米级的流体动力学效应导致ATP合酶旋转,并最终导致ATP释放到水溶液中。该模型还解释了用于调节跨膜运输的跨膜质子动力的产生,但是对于电子运输和ATP合成的耦合不是必需的。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号