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叶绿体Tat途径利用跨膜电势作为能源。

The chloroplast Tat pathway utilizes the transmembrane electric potential as an energy source.

作者信息

Braun Nikolai A, Davis Andrew W, Theg Steven M

机构信息

Department of Plant Biology, University of California, Davis, CA 95616, USA.

出版信息

Biophys J. 2007 Sep 15;93(6):1993-8. doi: 10.1529/biophysj.106.098731. Epub 2007 May 18.

Abstract

The thylakoid membrane, located inside the chloroplast, requires proteins transported across it for plastid biogenesis and functional photosynthetic electron transport. The chloroplast Tat translocator found on thylakoids transports proteins from the plastid stroma to the thylakoid lumen. Previous studies have shown that the chloroplast Tat pathway is independent of NTP hydrolysis as an energy source and instead depends on the thylakoid transmembrane proton gradient to power protein translocation. Because of its localization on the same membrane as the proton motive force-dependent F(0)F(1) ATPase, we believed that the chloroplast Tat pathway also made use of the thylakoid electric potential for transporting substrates. By adjusting the rate of photosynthetic proton pumping and by utilizing ionophores, we show that the chloroplast Tat pathway can also utilize the transmembrane electric potential for protein transport. Our findings indicate that the chloroplast Tat pathway is likely dependent on the total protonmotive force (PMF) as an energy source. As a protonmotive-dependent device, certain predictions can be made about structural features expected to be found in the Tat translocon, specifically, the presence of a proton well, a device in the membrane that converts electrical potential into chemical potential.

摘要

类囊体膜位于叶绿体内部,质体生物发生和功能性光合电子传递需要蛋白质穿过该膜。类囊体上发现的叶绿体Tat转运体将蛋白质从质体基质转运到类囊体腔。先前的研究表明,叶绿体Tat途径不依赖NTP水解作为能量来源,而是依赖类囊体跨膜质子梯度为蛋白质转运提供动力。由于其定位于与质子动力依赖的F(0)F(1) ATP合酶相同的膜上,我们认为叶绿体Tat途径也利用类囊体电势来转运底物。通过调节光合质子泵浦速率并利用离子载体,我们表明叶绿体Tat途径也可以利用跨膜电势进行蛋白质转运。我们的研究结果表明,叶绿体Tat途径可能依赖总质子动力(PMF)作为能量来源。作为一种质子动力依赖装置,可以对Tat转运体中预期发现的结构特征做出某些预测,具体而言,即质子阱的存在,质子阱是膜中一种将电势转化为化学势的装置。

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