Sugawara K, Yoshizawa Y, Tzeng S, Epstein W L, Fukuyama K
Department of Dermatology, University of California, San Francisco 94143, USA.
Anal Biochem. 1998 Dec 1;265(1):92-6. doi: 10.1006/abio.1998.2925.
A method is described for the direct colorimetric determination of citrulline residues in proteins based on the reaction with diacetylmonoxime in the presence of lower concentrations of sulfuric acid. The reduced sensitivity due to the lower acid concentration was overcome by the addition of ferric chloride which also contributed to the color stabilization. Insoluble proteins or proteins resulting in turbidity can be analyzed following partial hydrolysis of those with enzyme or acid. The molar absorption coefficient (epsilon) for citrulline at 464 nm was 2.8 x 10(4). The method enabled us to determine low levels of protein-bound citrulline which are beyond the limitations of conventional methods using an amino acid analyzer. We determined the citrulline contents in the cornified cells of the epidermis of newborn rats, as well as soybean trypsin inhibitor.
本文描述了一种基于在低浓度硫酸存在下与二乙酰一肟反应直接比色测定蛋白质中瓜氨酸残基的方法。通过添加氯化铁克服了由于较低酸浓度导致的灵敏度降低,氯化铁还有助于颜色稳定。不溶性蛋白质或导致浑浊的蛋白质在用酶或酸部分水解后可以进行分析。瓜氨酸在464nm处的摩尔吸收系数(ε)为2.8×10⁴。该方法使我们能够测定低水平的蛋白质结合瓜氨酸,这是使用氨基酸分析仪的传统方法所无法达到的。我们测定了新生大鼠表皮角质形成细胞以及大豆胰蛋白酶抑制剂中的瓜氨酸含量。