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哺乳动物金属硫蛋白的质子核磁共振研究。

Proton nuclear magnetic resonance studies of mammalian metallothioneins.

作者信息

Mitsumori F, Tohyama C

出版信息

J Biochem. 1984 Aug;96(2):533-43. doi: 10.1093/oxfordjournals.jbchem.a134865.

Abstract

Proton nuclear magnetic resonance studies of various mammalian metallothioneins are described. Metallothioneins-1 and 2, isolated from rat and rabbit, and also metallothionein-2, from humans, were investigated. Proton NMR spectra showed that mammalian metallothioneins containing Cd have similar tertiary structures regardless of their sources. On the other hand, metallothioneins containing both Cd and Zn have a slightly different conformation from those containing Cd alone. Almost all methyl resonances of Cd-metallothioneins were assigned to those of Met, Ile, Leu, Val, Thr, and Ala residues by NMR double resonance techniques, pH titration, and the spectral comparison of these metallothioneins. alpha-Proton resonances of Ala residues were classified into two groups, one of which arose around 4.1 ppm, the other around 4.4 ppm. Moreover, the number of alpha-proton resonances around 4.1 ppm and 4.4 ppm agreed with the number of Ala residues in the COOH-terminal and NH2-terminal domains of the metallothionein, respectively. This finding suggests that the chemical shift values of alpha-protons of Ala residues are reflective of the domain structure of the metallothioneins.

摘要

描述了对各种哺乳动物金属硫蛋白的质子核磁共振研究。研究了从大鼠和兔子中分离出的金属硫蛋白-1和2,以及从人类中分离出的金属硫蛋白-2。质子核磁共振光谱表明,含镉的哺乳动物金属硫蛋白无论来源如何,都具有相似的三级结构。另一方面,同时含有镉和锌的金属硫蛋白与仅含镉的金属硫蛋白具有略有不同的构象。通过核磁共振双共振技术、pH滴定以及这些金属硫蛋白的光谱比较,几乎所有镉-金属硫蛋白的甲基共振都被归属于甲硫氨酸、异亮氨酸、亮氨酸、缬氨酸、苏氨酸和丙氨酸残基的甲基共振。丙氨酸残基的α-质子共振分为两组,一组出现在约4.1 ppm处,另一组出现在约4.4 ppm处。此外,约4.1 ppm和4.4 ppm处的α-质子共振数量分别与金属硫蛋白COOH末端和NH2末端结构域中的丙氨酸残基数量一致。这一发现表明,丙氨酸残基α-质子的化学位移值反映了金属硫蛋白的结构域结构。

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