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抑制剂混合物的作用以及不同阴离子对铜蓝蛋白氧化酶活性的具体影响。

The effects of inhibitor mixtures and the specific effects of different anions on the oxidase activity of caeruloplasmin.

作者信息

Curzon G, Speyer B E

出版信息

Biochem J. 1968 Aug;109(1):25-34. doi: 10.1042/bj1090025.

Abstract
  1. The interpretation of the effects of mixtures of inhibitors on enzymes is considered. 2. The effects of inhibitor mixtures on caeruloplasmin were determined. 3. Fluoride, chloride and cyanate inhibit at one type of site (alpha), whereas bromide and iodide inhibit at another type (beta) present in the same enzyme intermediate. 4. Effects of inhibitor mixtures containing azide or cyanide are consistent with previous indications (Speyer & Curzon, 1968) that these ligands form inhibited complexes with different enzyme intermediates. 5. Isobols of halides or of cyanate with azide indicate that azide inhibits caeruloplasmin by bridging two alpha sites, these being reduced copper atoms. 6. Iodide and cyanate give hyperbolic plots of 1/v against [I]. 7. It is suggested that in the cyanate-inhibited complex the inhibitor binds to a reduced copper atom (alpha site) but that binding of cyanate at another copper atom is sterically prevented. It is suggested that the less bulky alpha-site inhibitors, fluoride and chloride, cause complete inhibition by binding to both of these copper atoms, which can also be bridged by a single azide group. 8. Each halide shows a pattern of effects on caeruloplasmin that is qualitatively distinct from that of other halides.
摘要
  1. 本文考虑了抑制剂混合物对酶作用的解释。2. 测定了抑制剂混合物对铜蓝蛋白的作用。3. 氟化物、氯化物和氰酸盐在一种类型的位点(α)上起抑制作用,而溴化物和碘化物在同一酶中间体中存在的另一种类型(β)的位点上起抑制作用。4. 含有叠氮化物或氰化物的抑制剂混合物的作用与先前的研究结果(Speyer & Curzon,1968)一致,即这些配体与不同的酶中间体形成抑制性复合物。5. 卤化物或氰酸盐与叠氮化物的等效线表明,叠氮化物通过桥接两个α位点来抑制铜蓝蛋白,这两个位点为还原态铜原子。6. 碘化物和氰酸盐给出了1/v对[I]的双曲线图。7. 有人提出,在氰酸盐抑制的复合物中,抑制剂与一个还原态铜原子(α位点)结合,但在另一个铜原子上氰酸盐的结合受到空间位阻的阻碍。有人提出,体积较小的α位点抑制剂,即氟化物和氯化物,通过与这两个铜原子结合而导致完全抑制,这两个铜原子也可以由单个叠氮基团桥接。8. 每种卤化物对铜蓝蛋白的作用模式在性质上与其他卤化物不同。

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Biochem J. 1966 Aug;100(2):295-302. doi: 10.1042/bj1000295.
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Eur J Biochem. 1972 Jun 9;27(3):572-7. doi: 10.1111/j.1432-1033.1972.tb01874.x.

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