Eamon P Breen, Wayne Pilgrim, Kieran J Clarke, Cristy Yssel, Mark Farrell, Jian Zhou, Paul V Murphy, Richard K Porter
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引用次数: 4
Abstract
We previously demonstrated that uncoupling protein 1 activity, as measured in isolated brown adipose tissue mitochondria (and as a native protein reconstituted into liposome membranes), was not activated by the non-flippable modified saturated fatty acid, glucose-O-ω-palmitate, whereas activity was stimulated by palmitate alone (40 nM free final concentration). In this study, we investigated whether fatty acid chain length had any bearing on the ability of glucose-O-ω-fatty acids to activate uncoupling protein 1. Glucose-O-ω-saturated fatty acids of various chain lengths were synthesized and tested for their potential to activate GDP-inhibited uncoupling protein 1-dependent oxygen consumption in brown adipose tissue mitochondria, and the results were compared with equivalent non-modified fatty acid controls. Here we demonstrate that laurate (12C), palmitate (16C) and stearate (18C) could activate GDP-inhibited uncoupling protein 1-dependent oxygen consumption in brown adipose tissue mitochondria, whereas there was no activation with glucose-O-ω-laurate (12C), glucose-O-ω-palmitate (16C), glucose-O-ω-stearate (18C), glucose-O-ω-arachidate (20C) or arachidate alone. We conclude that non-flippable fatty acids cannot activate uncoupling protein 1 irrespective of chain length. Our data further undermine the cofactor activation model of uncoupling protein 1 function but are compatible with the model that uncoupling protein 1 functions by flipping long-chain fatty acid anions.
我们之前证明,解偶联蛋白1的活性,在分离的棕色脂肪组织线粒体中测量(以及作为脂质体膜重组的天然蛋白),不被不可翻转的改性饱和脂肪酸葡萄糖-ω-棕榈酸酯激活,而活性被单独的棕榈酸酯(40 nM游离终浓度)刺激。在这项研究中,我们研究了脂肪酸链长度是否与葡萄糖ω脂肪酸激活解偶联蛋白1的能力有关。合成了不同链长的葡萄糖-ω饱和脂肪酸,并测试了它们激活棕色脂肪组织线粒体中受gdp抑制的解偶联蛋白1依赖的氧消耗的潜力,并将结果与等效的未修饰脂肪酸对照进行了比较。在这里,我们证明月桂酸酯(12C)、棕榈酸酯(16C)和硬脂酸酯(18C)可以激活棕色脂肪组织线粒体中受gdp抑制的解偶联蛋白1依赖的氧气消耗,而葡萄糖- o -ω-月桂酸酯(12C)、葡萄糖- o -ω-棕榈酸酯(16C)、葡萄糖- o -ω-硬脂酸酯(18C)、葡萄糖- o -ω-花生酯(20C)或单独使用花生酯则没有激活作用。我们得出结论,无论链长如何,不可翻转脂肪酸都不能激活解偶联蛋白1。我们的数据进一步破坏了解偶联蛋白1功能的辅因子激活模型,但与解偶联蛋白1通过翻转长链脂肪酸阴离子起作用的模型兼容。