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利什曼原虫线粒体tRNA导入复合物由tRNA触发的ATP水解及膜电位的产生

tRNA-triggered ATP hydrolysis and generation of membrane potential by the leishmania mitochondrial tRNA import complex.

作者信息

Bhattacharyya Subhendra Nath, Adhya Samit

机构信息

Genetic Engineering Laboratory, Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Calcutta 700032, India.

出版信息

J Biol Chem. 2004 Mar 19;279(12):11259-63. doi: 10.1074/jbc.C300540200. Epub 2004 Jan 22.

Abstract

Translocation of tRNAs across mitochondrial membranes is a receptor-mediated active transport process requiring ATP. A large tRNA import complex from the inner membrane of Leishmania mitochondria catalyzes translocation into phospholipid vesicles. In this reconstituted system, the import substrate tRNA(Tyr)(GUA) specifically stimulated hydrolysis of ATP within the vesicles, with the subsequent generation of a membrane potential by pumping out of protons, as shown by the protonophore-sensitive uptake of the potential-sensitive dye rhodamine 123. Generation of membrane potential was dependent on ATP hydrolysis, and inhibited by oligomycin, recalling the proton-translocation mechanism of the respiratory F(1)-F(0)-ATPase. For translocation of tRNA, ATP could be replaced by low pH of the medium, but proton-dependent import was resistant to oligomycin. Moreover, ATP hydrolysis, generation of membrane potential and tRNA uptake were inhibited by carboxyatractyloside, a specific inhibitor of mitochondrial ATP-ADP translocase, implying an ATP requirement within the vesicles. These observations imply a gating mechanism in which tRNA, on binding to its receptor, triggers the energetic activation of the complex, leading to the opening of import channels.

摘要

转运RNA(tRNA)穿过线粒体膜的过程是一种受体介导的主动运输过程,需要ATP参与。利什曼原虫线粒体内膜上的一个大型tRNA导入复合物催化其转运到磷脂囊泡中。在这个重组系统中,导入底物tRNA(Tyr)(GUA)特异性地刺激囊泡内ATP的水解,随后通过质子泵出产生膜电位,这可通过质子载体敏感的电位敏感染料罗丹明123的摄取来显示。膜电位的产生依赖于ATP水解,并受到寡霉素的抑制,这让人联想到呼吸F(1)-F(0)-ATP酶的质子转运机制。对于tRNA的转运,ATP可以被培养基的低pH值所替代,但质子依赖性导入对寡霉素具有抗性。此外,ATP水解、膜电位的产生和tRNA摄取受到线粒体ATP-ADP转位酶的特异性抑制剂羧基苍术苷的抑制,这意味着囊泡内需要ATP。这些观察结果暗示了一种门控机制,即tRNA与受体结合后,触发复合物的能量激活,导致导入通道打开。

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