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人2-巨球蛋白的硫还原。亚基结构。

Thio reduction of human 2 -macroglobulin. The subunit structure.

作者信息

Jones J M, Creeth J M, Kekwick R A

出版信息

Biochem J. 1972 Mar;127(1):187-97. doi: 10.1042/bj1270187.

Abstract
  1. Human alpha(2)-macroglobulin was prepared from a fraction obtained during the large-scale separation of normal human plasma proteins for clinical use. 2. Sedimentation-equilibrium measurements indicated a molecular weight of 725000. A value of 18.1S was obtained for s(0) (20,w). 3. The dissociation that occurs in the pH range 4.5-2.5 and in the region of neutrality in urea-containing solutions is consistent with a dimeric structure of the molecule. 4. The effects of the thiol reagents mercaptoethanol, mercaptoethylamine and N-acetylcysteine were investigated over a range of experimental conditions. Distinct components having sedimentation coefficients of 15, 12 and 8.5S were identified. 5. Conditions were found under which limited reduction with thiol liberated a subunit with a molecular weight approximately one-quarter of that of the intact molecule. This subunit retains the serological specificity of the whole molecule.
摘要
  1. 人α(2)-巨球蛋白是从大规模分离正常人血浆蛋白以供临床使用过程中获得的一个组分制备而来。2. 沉降平衡测量表明分子量为725000。s(0)(20,w)的值为18.1S。3. 在pH值4.5 - 2.5范围内以及含尿素溶液的中性区域发生的解离与该分子的二聚体结构一致。4. 在一系列实验条件下研究了巯基试剂巯基乙醇、巯基乙胺和N-乙酰半胱氨酸的作用。鉴定出沉降系数分别为15、12和8.5S的不同组分。5. 发现了这样的条件,在此条件下用巯基进行有限度还原可释放出一个亚基,其分子量约为完整分子的四分之一。该亚基保留了整个分子的血清学特异性。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fc6/1178573/3c8f2817acb3/biochemj00634-0194-a.jpg

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