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过氧化物酶催化酪氨酸碘化的动力学及机制

Kinetics and mechanism of the peroxidase-catalyzed iodination of tyrosine.

作者信息

Sun W, Dunford H B

机构信息

Department of Chemistry, University of Alberta, Edmonton, Canada.

出版信息

Biochemistry. 1993 Feb 9;32(5):1324-31. doi: 10.1021/bi00056a018.

Abstract

The kinetics of iodination of tyrosine by hydrogen peroxide and iodide, catalyzed by both horseradish peroxidase (HRP) and lactoperoxidase (LPO), were studied. The initial rates of formation of both molecular I2 and monoiodotyrosine (MIT) were measured with stopped flow techniques. The following reactions occur in both systems. Enzymatic: FeIII + H2O2-->Fev = O + H2O; Fev = O + I(-)-->FeIII-O-I-; FeIII-O-I- + H(+)-->FeIII + HOI; FeIII-O-I- + I- + H(+)-->FeIII + I2 + HO-. Iodine equilibria: I2 + I-<-->I3-; I2 + H2O<-->HOI + I- + H+. Nonenzymatic iodination, one or both of the following: Tyr + HOI-->MIT + H2O; Tyr + I2-->MIT + I- + H+, where FeIII is native peroxidase, Fev = O is compound I and Tyr is tyrosine. The big difference in the two systems is that the following reaction also occurs with LPO: FeIII-O-I- + Tyr-->MIT + FeIII + HO-, which is the dominant mechanism of iodination for the mammalian enzyme. The overall rate of formation of MIT is about 10 times faster for LPO compared to HRP under comparable conditions. A small decrease in rate occurs when D-tyrosine is substituted for L-tyrosine in the LPO reaction. Thus LPO has a tyrosine binding site near the heme. A kinetically controlled maximum is observed in I3- concentration. Once equilibrium is established, I2 is the dominant form of inorganic iodine in solution. However, hypoiodous acid may be the inorganic iodination reagent.

摘要

研究了辣根过氧化物酶(HRP)和乳过氧化物酶(LPO)催化下,过氧化氢和碘化物对酪氨酸碘化的动力学。采用停流技术测定了分子碘(I₂)和一碘酪氨酸(MIT)的初始生成速率。两个体系中均发生以下反应。酶促反应:FeIII + H₂O₂→Fev = O + H₂O;Fev = O + I⁻→FeIII - O - I⁻;FeIII - O - I⁻ + H⁺→FeIII + HOI;FeIII - O - I⁻ + I⁻ + H⁺→FeIII + I₂ + HO⁻。碘平衡反应:I₂ + I⁻⇌I₃⁻;I₂ + H₂O⇌HOI + I⁻ + H⁺。非酶促碘化反应,以下一个或两个反应:Tyr + HOI→MIT + H₂O;Tyr + I₂→MIT + I⁻ + H⁺,其中FeIII是天然过氧化物酶,Fev = O是化合物I,Tyr是酪氨酸。两个体系的最大差异在于,LPO还会发生以下反应:FeIII - O - I⁻ + Tyr→MIT + FeIII + HO⁻,这是哺乳动物酶碘化反应的主要机制。在可比条件下,LPO催化生成MIT的总速率比HRP快约10倍。在LPO反应中,用D - 酪氨酸替代L - 酪氨酸时,反应速率略有下降。因此,LPO在血红素附近有一个酪氨酸结合位点。在I₃⁻浓度上观察到一个动力学控制的最大值。一旦建立平衡,I₂是溶液中无机碘的主要形式。然而,次碘酸可能是无机碘化试剂。

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