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猪肌肉腺苷酸激酶及其底物复合物的质子磁共振谱

Proton magnetic resonance spectra or porcine muscle adenylate kinase and substrate complexes.

作者信息

McDonald G G, Cohn M

出版信息

J Biol Chem. 1975 Sep 10;250(17):6947-54.

PMID:239953
Abstract

Porcine muscle adenylate kinase with a molecular weight of 22,000 has 2 histidine, 5 phenylalanine, 7 tyrosine, and no tryptophan residues. The effect of pH, substrate, and the paramagnetic manganous ion on the proton magnetic resonance spectrum of the enzyme, particularly the aromatic region, has been investigated at 220 MHz. The well resolved C2 proton peaks of the 2 histidine residues have been individually assigned to His-36 and His-189 by comparison with the spectrum of the carp muscle enzyme which has only one C2 proton peak and only 1 histidine residue, 36. The chemical shift of the peak designated C2-H of His-36 in the porcine enzyme has a normal titration curve with a pKalpha = 6.3 but the peak for His-189 is not titratable in the pH range 5.8 to 8.1. The pKalpha of the single His-36 of the carp enzyme is similar to that of His-36 of the porcine enzyme. Changes in pH, particularly at low pH, also affect the chemical shifts of the tyrosine residues. Occupation of either the monophosphate site by AMP or the triphosphate site by ATP or GTP causes a downfield shift of the C2-H of His-36, and the equilibrium mixture causes an even greater shift, but no shift in the C2-H of His-189. The substrates also induce changes in the chemical shifts in the phenylalanine-tyrosine region of the spectrum. Tentative assignments of the highest and lowest field peaks in this region have been made based on the three-dimensional structure determined by x-ray crystallography. On the basis of these assignments, it is concluded that Phe-183 is unperturbed by substrate binding but that Tyr-153 or -154 at the hinge of the molecule, are perturbed. The C2-H of adenine and C8-H of adenine or guanine of the bound substrates were also observed; those of AMP are unperturbed but C2-H of ATO is shifted downfield and the C8-H of ATP and GTP are shifted upfield. The paramagnetic manganous ion had no effect on the spectrum at Mn(II) to enzyme ratios below 1:10; above this ratio, a general broadening was observed...

摘要

分子量为22,000的猪肌肉腺苷酸激酶含有2个组氨酸、5个苯丙氨酸、7个酪氨酸,不含色氨酸残基。在220兆赫下研究了pH值、底物和顺磁性锰离子对该酶质子磁共振谱的影响,特别是芳香区的影响。通过与仅具有一个C2质子峰和仅1个组氨酸残基(36)的鲤鱼肌肉酶的谱图比较,已将2个组氨酸残基分辨良好的C2质子峰分别指定为His - 36和His - 189。猪酶中His - 36的指定为C2 - H的峰具有正常的滴定曲线,pKα = 6.3,但His - 189的峰在pH范围5.8至8.1内不可滴定。鲤鱼酶的单个His - 36的pKα与猪酶的His - 36相似。pH值的变化,特别是在低pH值时,也会影响酪氨酸残基的化学位移。AMP占据单磷酸位点或ATP或GTP占据三磷酸位点会导致His - 36的C2 - H向低场移动,平衡混合物会导致更大的移动,但His - 189的C2 - H没有移动。底物还会引起谱图中苯丙氨酸 - 酪氨酸区域化学位移的变化。基于通过X射线晶体学确定的三维结构,对该区域中最高和最低场峰进行了初步归属。基于这些归属,得出结论:Phe - 183不受底物结合的干扰,但分子铰链处的Tyr - 153或 - 154受到干扰。还观察到结合底物的腺嘌呤的C2 - H和腺嘌呤或鸟嘌呤的C8 - H;AMP的那些不受干扰,但ATP的C2 - H向低场移动,ATP和GTP的C8 - H向上场移动。在Mn(II)与酶的比例低于1:10时,顺磁性锰离子对谱图没有影响;高于此比例时,观察到普遍的谱线展宽……

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