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Quantitative Determination of Biological Sulfhydryl Groups by Postcolumn Derivatization and Elucidation of Microheterogeneity of Serum Albumins

机译:柱后衍生化和血清白蛋白微异质性的定量测定生物巯基基团

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A quantitative analytical system for biological sulfhydryl compounds has been developed using an ion-pair reagent with isocratic elution and an on-line postcolumn derivatization with Ellman-type reagents. As human or bovine serum albumin has 35 cysteinyl residues, one cysteinyl residue exists as a free sulfhydryl moiety, and this gives rise to the microheterogeneity in serum albumin. Here we report for the first lime the quantitative characterization of the microheterogeneity of serum albumin. Cysteine was found to be the major molecule attached to the sulfydryl group of the serum albumins. Although glutathione could not be detected, the Cys-Gly element of glutathione was found. Freshly prepared human serum albumin from healthy volunteers contained 0.46 nmol of Cys/mL of serum, 0.24 umol of Cys-Gly/mL of serum, Rd very small amounts of glutathione (0.02 nmol/mL).
机译:已经开发了一种使用等离子洗脱的离子对试剂和用Ellman型试剂进行柱后在线衍生化的生物巯基化合物的定量分析系统。由于人或牛血清白蛋白具有35个半胱氨酰基残基,一个半胱氨酰基残基作为游离巯基部分存在,这引起了血清白蛋白的微异质性。在这里,我们首先报道了血清白蛋白微异质性的定量表征。发现半胱氨酸是附着在血清白蛋白的巯基上的主要分子。尽管无法检测到谷胱甘肽,但发现了谷胱甘肽的Cys-Gly元素。来自健康志愿者的新鲜制备的人血清白蛋白包含0.46 nmol的Cys / mL血清,0.24 umol的Cys-Gly / mL血清,Rd极少量的谷胱甘肽(0.02 nmol / mL)。

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