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β146位组氨酸残基在血红蛋白碱性玻尔效应中的作用。

Role of the beta 146 histidyl residue in the alkaline Bohr effect of hemoglobin.

作者信息

Russu I M, Ho N T, Ho C

出版信息

Biochemistry. 1980 Mar 4;19(5):1043-52. doi: 10.1021/bi00546a033.

Abstract

High-resolution proton nuclear magnetic resonance spectroscopy has been used to investigate the effects of inorganic anions, such as phosphate or chloride, on the alkaline Bohr effect of normal human adult hemoglobin. By monitoring the chemical shift of the C2 proton of the beta 146 histidyl residue as a function of pH, we have determined its pK values in both ligated and unligated forms. In the presence of 0.1 M Bis-Tris buffer (with chloride ion concentration ranging from 0.005 to 0.06 M) in D2O at 27 degrees C, the pK value of the beta 146 histidine of deoxyhemoglobin is 7.98 +/- 0.03 and that of (carbon monoxy)hemoglobin is 7.85 +/- 0.03. However, in the presence of 0.2 M phosphate and 0.2 M NaCl in D2O at 27 degrees C, the corresponding pK values are 8.08 and 7.14, as previously reported by this laboratory [Kilmartin, J. V., Breen, J. J., Roberts, G. C. K., & Ho, C. (1973) Proc. Natl. Acad. Sci. U.S.A. 70, 1246-1249]. This large difference in the pK value between the deoxy and carbon monoxy forms in the presence of 0.2 M phosphate and 0.2 M NaCl was interpreted as direct support for (1) the breaking of an intrasubunit salt bridge between beta 146 histidine and beta 94 aspartate when the hemoglobin molecule undergoes the quaternary structural transition as proposed by Perutz [Perutz, M. F. (1970) Nature (London) 228, 726-739] and (2) Perutz's suggestion that the beta 146 histidine is one of the amino acid residues responsible for the alkaline Bohr effect. The absence of a large change in the pK value of the beta 146 histidine in the presence of 0.1 M Bis-Tris buffer implies that (1) the above-mentioned intrasubunit salt bridge is not broken in going from the deoxy to the carbon monoxy form and (2) the beta 146 histidyl residue does not contribute significantly to the alkaline Bohr effect under these conditions. We have also found that in measuring the oxygen affinity of hemoglobin as a function of pH in the presence of 0.1 M Bis-Tris or 0.2 M phosphate plus 0.2 M NaCl (both in D2O), there is no significant difference in the alkaline Bohr effect in these two media. Hence, our results suggest that the detailed molecular mechanism for the Bohr effect depends on the experimental conditions.

摘要

高分辨率质子核磁共振光谱已被用于研究无机阴离子(如磷酸盐或氯离子)对正常成人血红蛋白碱性玻尔效应的影响。通过监测β146组氨酸残基C2质子的化学位移随pH的变化,我们确定了其在结合态和未结合态下的pK值。在27℃的D2O中,存在0.1M的双(2-羟乙基)氨基三(羟甲基)甲烷缓冲液(氯离子浓度范围为0.005至0.06M)时,脱氧血红蛋白β146组氨酸的pK值为7.98±0.03,而(一氧化碳)血红蛋白的pK值为7.85±0.03。然而,在27℃的D2O中,存在0.2M磷酸盐和0.2M氯化钠时,相应的pK值分别为8.08和7.14,如本实验室先前报道[Kilmartin, J. V., Breen, J. J., Roberts, G. C. K., & Ho, C. (1973) Proc. Natl. Acad. Sci. U.S.A. 70, 1246 - 1249]。在存在0.2M磷酸盐和0.2M氯化钠的情况下,脱氧态和一氧化碳结合态之间pK值的巨大差异被解释为直接支持以下两点:(1)当血红蛋白分子经历佩鲁茨提出的四级结构转变时,β146组氨酸和β94天冬氨酸之间的亚基内盐桥断裂[佩鲁茨,M. F. (1970) Nature (London) 228, 726 - 739];(2)佩鲁茨的观点,即β146组氨酸是负责碱性玻尔效应的氨基酸残基之一。在存在0.1M双(2-羟乙基)氨基三(羟甲基)甲烷缓冲液的情况下,β146组氨酸的pK值没有显著变化,这意味着:(1)从脱氧态到一氧化碳结合态时,上述亚基内盐桥没有断裂;(2)在这些条件下,β146组氨酸残基对碱性玻尔效应的贡献不大。我们还发现,在0.1M双(2-羟乙基)氨基三(羟甲基)甲烷或0.2M磷酸盐加0.2M氯化钠(均在D2O中)存在的情况下,测量血红蛋白的氧亲和力随pH的变化时,这两种介质中的碱性玻尔效应没有显著差异。因此,我们的结果表明,玻尔效应的详细分子机制取决于实验条件。

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