Jezek P, Orosz D E, Modriansky M, Garlid K D
Institute of Physiology, Czech Academy of Sciences, Prague.
J Biol Chem. 1994 Oct 21;269(42):26184-90.
The uncoupling protein generates heat by catalyzing electrophoretic proton transport across the inner membrane of brown adipose tissue mitochondria. It also transports Cl- and other monovalent anions, and both proton and anion transport are inhibited by purine nucleotides. Several long-standing hypotheses bear on specific aspects of Cl- transport, H+ transport, and nucleotide gating mechanisms in uncoupling protein. We reevaluated these hypotheses in mitochondria and liposomes reconstituted with purified uncoupling protein; GDP inhibition is strictly noncompetitive with Cl- and unaffected by either transmembrane electrical potential or fatty acids. The Km and Vmax values for Cl- are independent of pH, arguing against a common binding site for Cl- and OH- ions. Cl- transport was inhibited by fatty acids and stimulated by fatty acid removal, refuting the consensus hypothesis that there is no interaction between fatty acids and anion transport through uncoupling protein. These results support a mechanism in which the transport pathway for anions is identical with the fatty acid binding site and distinct from the nucleotide binding site.
解偶联蛋白通过催化质子跨棕色脂肪组织线粒体内膜的电泳转运来产生热量。它还能转运氯离子和其他单价阴离子,质子和阴离子的转运均受嘌呤核苷酸抑制。几个长期存在的假说涉及解偶联蛋白中氯离子转运、氢离子转运和核苷酸门控机制的特定方面。我们在用纯化的解偶联蛋白重构的线粒体和脂质体中重新评估了这些假说;GDP抑制对氯离子严格呈非竞争性,且不受跨膜电势或脂肪酸的影响。氯离子的Km和Vmax值与pH无关,这与氯离子和氢氧根离子存在共同结合位点的观点相悖。氯离子转运受脂肪酸抑制,脂肪酸去除后则受到刺激,这驳斥了脂肪酸与通过解偶联蛋白的阴离子转运之间不存在相互作用的普遍假说。这些结果支持了一种机制,即阴离子的转运途径与脂肪酸结合位点相同,与核苷酸结合位点不同。