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棕色脂肪组织线粒体中核苷酸结合位点的掩盖性质。内源性三磷酸腺苷的参与。

Nature of the masking of nucleotide-binding sites in brown adipose tissue mitochondria. Involvement of endogenous adenosine triphosphate.

作者信息

Huang S G, Klingenberg M

机构信息

Institute of Physical Biochemistry, University of Munich, Germany.

出版信息

Eur J Biochem. 1995 May 1;229(3):718-25. doi: 10.1111/j.1432-1033.1995.tb20519.x.

Abstract

Binding of the fluorescent nucleotide derivative 2'-O-dansyl GTP and purine nucleotides to brown adipose tissue mitochondria from hamster was studied. 2'-O-Dansyl GTP binds with enhanced fluorescence to the uncoupling protein (UCP) in the mitochondria, similar to the isolated protein. The fluorescence signal showed biphasic fast and slow increases. Treatment of the mitochondria with an anion exchanger (Dowex) increased the total fluorescence but decreased the slower phase. The biphasic fluorescence response was restored by incubation with only 1 microM ATP, indicating that residual bound ATP may be responsible for the observed slow phase. The binding of [14C]GTP and GDP also increased after Dowex treatment. The dissociation of bound [14C]ATP but not of bound [14C]ADP was slow and apparently limited the binding assays. Short incubation (5 min) resulted in a curvature of the Scatchard plot, where the 'high-affinity sites' correspond to the free UCP sites; GDP had apparently higher affinity than GTP. Dowex treatment and incubation for 60 min produced a more linear Scatchard plot. Under such conditions, one measures the maximal UCP-binding sites (1.2 mumol/g protein); GTP exhibited higher affinity (Kd = 0.64 microM) than GDP (Kd = 3.1 microM). Acute cold adaptation (40 min at 4 degrees C) of hamsters caused an increase by over 40% of [14C]GTP binding, as compared to the control warm-(28 degrees C)-adapted animals. Dowex treatment completely abolishes this unmasking/masking effect, where both mitochondria had identical binding capacity and affinity for GTP. The inhibition by purine nucleotides of H+ transport as measured by potassium-acetate-induced mitochondrial swelling was dependent on the incubation time. Diphosphates inhibited faster and triphosphates required longer incubation (10 min) but inhibited more strongly. A linear correlation between the mitochondrial swelling rate and GDP binding was observed for mitochondria with depleted endogenous ATP or with added ATP. These data indicate that residual bound ATP from the tissue is responsible for the masking phenomenon.

摘要

研究了荧光核苷酸衍生物2'-O-丹磺酰鸟苷三磷酸(2'-O-dansyl GTP)和嘌呤核苷酸与仓鼠棕色脂肪组织线粒体的结合情况。2'-O-丹磺酰鸟苷三磷酸与线粒体中的解偶联蛋白(UCP)结合后荧光增强,这与分离出的蛋白情况类似。荧光信号呈现出快速和缓慢增加的双相性。用阴离子交换剂(Dowex)处理线粒体可增加总荧光,但会降低较慢的那一期。仅用1微摩尔/升的ATP孵育可恢复双相荧光反应,这表明残留结合的ATP可能是观察到的慢相的原因。Dowex处理后,[14C]GTP和GDP的结合也增加了。结合的[14C]ATP的解离缓慢,而结合的[14C]ADP的解离不明显,这显然限制了结合测定。短时间孵育(5分钟)导致Scatchard图呈曲线,其中“高亲和力位点”对应于游离的UCP位点;GDP的亲和力明显高于GTP。Dowex处理并孵育60分钟产生了更线性的Scatchard图。在这种条件下,可测定最大的UCP结合位点(1.2微摩尔/克蛋白);GTP的亲和力(解离常数Kd = 0.64微摩尔/升)高于GDP(Kd = 3.1微摩尔/升)。与对照的温暖(28摄氏度)适应动物相比,仓鼠急性冷适应(4摄氏度,40分钟)使[14C]GTP结合增加了40%以上。Dowex处理完全消除了这种暴露/掩盖效应,此时两种线粒体对GTP具有相同的结合能力和亲和力。通过醋酸钾诱导的线粒体肿胀来测量,嘌呤核苷酸对氢离子转运的抑制作用取决于孵育时间。二磷酸酯抑制更快,三磷酸酯需要更长的孵育时间(10分钟)但抑制作用更强。对于内源性ATP耗尽或添加了ATP的线粒体,观察到线粒体肿胀速率与GDP结合之间存在线性相关性。这些数据表明,组织中残留结合的ATP是掩盖现象的原因。

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