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血红蛋白与一氧化碳之间中间化合物的分离。

Isolation of intermediate compounds between hemoglobin and carbon monoxide.

作者信息

Perrella M, Benazzi L, Cremonesi L, Vesely S, Viggiano G, Rossi-Bernardi L

出版信息

J Biol Chem. 1983 Apr 10;258(7):4511-7.

PMID:6833264
Abstract

A human hemoglobin solution partially saturated with carbon monoxide was rapidly quenched at -25 degrees C into a hydro-organic buffer containing ferricyanide. Under the experimental conditions of pH, ionic strength, and buffer composition used in this work, it was found that the deoxy hemes were rapidly transformed into their met form, whereas practically no carbon monoxide-bound hemes were oxidized before the separation of the mixture from the oxidizing agent. As a preliminary step to the analysis of the resulting solution, carbonylhemoglobin solutions partially oxidized with ferricyanide were studied by isoelectric focusing at -25 degrees C under identical conditions. The relative position in the gel of all nine possible valence hybrids was established as follows (going from the anodic to the cathodic side of the gel) alpha CO2 beta CO2, (alpha CO beta +)(alpha CO beta CO) (alpha CO beta CO), (alpha CO2 beta +2), (alpha + beta CO), (alpha + beta +)-(alpha CO beta CO), (alpha + beta +)(alpha CO beta +), (alpha +2 beta CO2), (alpha + beta +)(alpha + beta CO), alpha +2 beta +2. When carbonylhemoglobin and methemoglobin were mixed in equal proportion at -25 degrees C and then analyzed by isoelectric focusing at the same temperature, it was found that the contribution of valence hybrids other than alpha CO2 beta CO2 and alpha +2 beta +2 to the total amount of hemoglobin in the gel was no more than 6%. When carbonylhemoglobin and deoxyhemoglobin were mixed in the same proportion and incubated at 20 degrees C so to allow the redistribution of the carbon monoxide molecules between all possible binding sites to occur, a substantially higher amount of valence hybrids, derived from the oxidation of intermediate compounds of hemoglobin with carbon monoxide, was found. The isoelectric focusing separation indicated the presence in the original solution of intermediate species other than carbonylhemoglobin and deoxyhemoglobin at a concentration of about 10% of the total.

摘要

一种部分被一氧化碳饱和的人血红蛋白溶液在-25℃下迅速淬灭到含有铁氰化物的水-有机缓冲液中。在本工作所使用的pH、离子强度和缓冲液组成的实验条件下,发现脱氧血红素迅速转化为高铁形式,而在将混合物与氧化剂分离之前,实际上没有与一氧化碳结合的血红素被氧化。作为分析所得溶液的初步步骤,在相同条件下于-25℃通过等电聚焦研究了用铁氰化物部分氧化的羰基血红蛋白溶液。所有九种可能的价态杂化物在凝胶中的相对位置如下确定(从凝胶的阳极侧到阴极侧):αCO₂βCO₂、(αCOβ⁺)(αCOβCO)、(αCOβCO)、(αCO₂β⁺²)、(α⁺βCO)、(α⁺β⁺)-(αCOβCO)、(α⁺β⁺)(αCOβ⁺)、(α⁺²βCO₂)、(α⁺β⁺)(α⁺βCO)、α⁺²β⁺²。当羰基血红蛋白和高铁血红蛋白在-25℃下等比例混合,然后在相同温度下通过等电聚焦进行分析时,发现除αCO₂βCO₂和α⁺²β⁺²之外的价态杂化物对凝胶中血红蛋白总量的贡献不超过6%。当羰基血红蛋白和脱氧血红蛋白按相同比例混合并在20℃下孵育,以使一氧化碳分子在所有可能的结合位点之间重新分布时,发现有大量来自血红蛋白与一氧化碳中间化合物氧化的价态杂化物。等电聚焦分离表明,原始溶液中除羰基血红蛋白和脱氧血红蛋白之外还存在中间物种,其浓度约占总量的10%。

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