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丙二酰辅酶A对大鼠肝脏线粒体外膜肉碱棕榈酰转移酶的抑制作用对化学诱导和温度诱导的膜流动性变化的敏感性。

Sensitivity of inhibition of rat liver mitochondrial outer-membrane carnitine palmitoyltransferase by malonyl-CoA to chemical- and temperature-induced changes in membrane fluidity.

作者信息

Kolodziej M P, Zammit V A

机构信息

Hannah Research Institute, Ayr, Scotland, UK.

出版信息

Biochem J. 1990 Dec 1;272(2):421-5. doi: 10.1042/bj2720421.

Abstract

We have tested the possibility that alterations in the fluidity of the outer membrane of rat liver mitochondria could result in changes in the sensitivity of overt carnitine palmitoyltransferase (CPT I) to malonyl-CoA [Zammit (1986) Biochem. Soc. Trans. 14. 676-679]. The sensitivity of CPT I to malonyl-CoA inhibition was measured by using highly purified mitochondrial outer membranes prepared from fed or 48 h-starved rats in the presence and absence of agents that increase membrane fluidity by perturbing membrane lipid order [benzyl alcohol, isoamyl alcohol (3-methylbutan-l-ol) and 2-(2-methoxyethoxy)ethyl-8-(cis-2-n-octylpropyl)octanoate (A2C)]. All these agents resulted in marked decreases in the ability of malonyl-CoA to inhibit CPT I. This effect was accompanied by a modest increase in the absolute activity of CPT I in the absence of malonyl-CoA when the short-chain alcohols were used, but not when A2C was used, suggesting that the effect of increased membrane fluidity to decrease the malonyl-CoA sensitivity of CPT I may occur independently from other actions that may affect more directly the active site of the enzyme. In confirmation of the potential importance of fluidity changes, we showed that a marked increase in sensitivity of CPT I to malonyl-CoA could be produced when assays were performed at lower temperatures than those normally employed. These observations are discussed in the context of the slowness of the changes in CPT I sensitivity to malonyl-CoA inhibition that are induced by physiological perturbations.

摘要

我们已经测试了大鼠肝脏线粒体外膜流动性的改变可能导致明显的肉碱棕榈酰转移酶(CPT I)对丙二酰辅酶A敏感性变化的可能性[扎米特(1986年),生物化学学会会报,14卷,676 - 679页]。通过使用从喂食或饥饿48小时的大鼠制备的高度纯化的线粒体外膜,在存在和不存在通过扰乱膜脂质有序性来增加膜流动性的试剂[苄醇、异戊醇(3 - 甲基丁醇)和2 - (2 - 甲氧基乙氧基)乙基 - 8 - (顺式 - 2 - 正辛基丙基)辛酸酯(A2C)]的情况下,测量CPT I对丙二酰辅酶A抑制的敏感性。所有这些试剂都导致丙二酰辅酶A抑制CPT I的能力显著降低。当使用短链醇时,在不存在丙二酰辅酶A的情况下,这种效应伴随着CPT I绝对活性的适度增加,但使用A2C时则没有,这表明膜流动性增加导致CPT I对丙二酰辅酶A敏感性降低的效应可能独立于其他可能更直接影响酶活性位点的作用而发生。为了证实流动性变化的潜在重要性,我们表明,当在比通常使用的温度更低的温度下进行测定时,CPT I对丙二酰辅酶A的敏感性会显著增加。这些观察结果在生理扰动诱导的CPT I对丙二酰辅酶A抑制敏感性变化缓慢的背景下进行了讨论。

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