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汉森碳酸酐酶组织化学检测法中的动力学、平衡及抑制作用:方法验证

Kinetics, equilibrium and inhibition in the Hansson histochemical procedure for carbonic anhydrase: a validation of the method.

作者信息

Maren T H

出版信息

Histochem J. 1980 Mar;12(2):183-90. doi: 10.1007/BF01024548.

Abstract

Quantitative analysis has been made of the reactions underlying the Hansson histochemical method for carbonic anhydrase, with a view toward resolving controversies that have arisen regarding its application and specificity. The basic event is the loss of CO2 from the surface of solutions containing HCO3(-), PO42(-) and cobalt at pH 6-8. Displacement of the equilibria H2CO3 in equilibrium CO2 to the right elevates the pH, and at 6.8 a cobalt precipitate is formed. When tissue containing carbonic anhydrase is floated on the surface, the loss of CO2 and elevation of pH is accelerated at the enzyme site, leading to increased cobalt deposits. These are converted to cobalt sulphide for visualization. Study of the changes of pH and CO2 equilibria during the reaction point strongly to the fact that enzymic activity is being measured by the cobalt localization. This activity is reduced or abolished by appropriate concentrations of acetazolamide (or other sulphonamide inhibitors of carbonic anhydrase) and the powerful inorganic inhibitor, cyanate (CNO-) ion.

摘要

已对汉森碳酸酐酶组织化学方法所涉及的反应进行了定量分析,目的是解决在其应用和特异性方面出现的争议。基本事件是在pH值为6 - 8的含有HCO3(-)、PO42(-)和钴的溶液表面CO2的损失。平衡H2CO3⇌CO2向右移动会提高pH值,在6.8时会形成钴沉淀。当含有碳酸酐酶的组织漂浮在表面时,酶作用部位CO2的损失和pH值的升高会加速,导致钴沉积增加。这些沉积会转化为硫化钴以便观察。对反应过程中pH值和CO2平衡变化的研究有力地表明,钴定位所测量的是酶活性。这种活性会被适当浓度的乙酰唑胺(或其他碳酸酐酶的磺胺类抑制剂)以及强效无机抑制剂氰酸根(CNO-)离子降低或消除。

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