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两种石胆酸结合蛋白的鉴定。将配体蛋白与谷胱甘肽S-转移酶B分离。

Identification of two lithocholic acid-binding proteins. Separation of ligandin from glutathione S-transferase B.

作者信息

Hayes J D, Strange R C, Percy-Robb I W

出版信息

Biochem J. 1979 Sep 1;181(3):699-708. doi: 10.1042/bj1810699.

Abstract
  1. Two lithocholic acid-binding proteins in rat liver cytosol, previously shown to have glutathione S-transferase activity, were resolved by CM-Sephadex chromatography. 2. Phenobarbitone administration resulted in induction of both binding proteins. 3. The two proteins had distinct subunit compositions indicating that they are dimers with mol.wts. 44 000 and 47 000. 4. The two lithocholic acid-binding proteins were identified by comparing their elution volumes from CM-Sephadex with those of purified ligandin and glutathione S-transferase B prepared by published procedures. Ligandin and glutathione S-transferase B were eluted separately, as single peaks of enzyme activity, at volumes equivalent to the two lithocholic acid-binding proteins. 5. Peptide 'mapping' revealed structural differences between the two proteins.
摘要
  1. 大鼠肝细胞溶质中的两种石胆酸结合蛋白,先前已证明具有谷胱甘肽S-转移酶活性,通过CM-葡聚糖凝胶层析进行分离。2. 给予苯巴比妥导致两种结合蛋白的诱导。3. 这两种蛋白具有不同的亚基组成,表明它们是分子量分别为44000和47000的二聚体。4. 通过比较它们从CM-葡聚糖凝胶上的洗脱体积与按照已发表方法制备的纯化的配体蛋白和谷胱甘肽S-转移酶B的洗脱体积,鉴定出这两种石胆酸结合蛋白。配体蛋白和谷胱甘肽S-转移酶B分别作为酶活性的单峰被洗脱,其洗脱体积与两种石胆酸结合蛋白相当。5. 肽“图谱”揭示了这两种蛋白之间的结构差异。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6a/1161210/e33d7bdd2307/biochemj00457-0199-a.jpg

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