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一种改进的用于胶原蛋白的 Bradford 蛋白质测定法。

An improved Bradford protein assay for collagen proteins.

作者信息

López J M, Imperial S, Valderrama R, Navarro S

机构信息

Gastroenterology Service, Hospital Clinic i Provincial, Barcelona, Spain.

出版信息

Clin Chim Acta. 1993 Oct 29;220(1):91-100. doi: 10.1016/0009-8981(93)90009-s.

Abstract

A modification of the protein determination method of Bradford adapted for collagen-rich samples is described. The use of Coomassie-based protein determination methods is limited by the great variation in colour yield obtained for different proteins. This is especially important in samples containing significant amounts of collagen where direct application of the methods of Lowry and Bradford results in underestimated values. Addition of small amounts of sodium dodecyl sulphate (SDS) (0.0035%) to the diluted solutions of Coomassie Brilliant Blue G used as dye reagent in the Bradford colorimetric assay caused a 4-fold increase in the colour response of three collagen proteins (Col I, III and IV) and a decrease in absorbance for various non-collagen proteins. The presence of SDS in the reagent did not result in a significant metachromatic shift of the collagen-dye complexes. This simple modification in the preparation of the reagent for the Bradford assay allows similar response curves to be obtained for collagen and non-collagen proteins, making the modified assay of potential use for protein determination in collagen-rich samples such as pancreatic extracts.

摘要

本文描述了一种适用于富含胶原蛋白样本的Bradford蛋白质测定方法的改进方法。基于考马斯亮蓝的蛋白质测定方法的应用受到不同蛋白质显色差异较大的限制。这在含有大量胶原蛋白的样本中尤为重要,因为直接应用Lowry法和Bradford法会导致结果低估。在Bradford比色法中用作染料试剂的考马斯亮蓝G稀释溶液中加入少量十二烷基硫酸钠(SDS)(0.0035%),可使三种胶原蛋白(I型、III型和IV型胶原)的颜色反应增加4倍,并降低各种非胶原蛋白的吸光度。试剂中SDS的存在不会导致胶原蛋白-染料复合物出现明显的异染性变化。Bradford测定试剂制备方法的这种简单改进使得胶原蛋白和非胶原蛋白能够获得相似的响应曲线,从而使改进后的测定方法可用于测定富含胶原蛋白的样本(如胰腺提取物)中的蛋白质。

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