Shindo H, Hayes M B, Cohen J S
J Biol Chem. 1976 May 10;251(9):2644-7.
One of the four titrating histidine ring C-2 proton resonances of bovine pancreatic ribonuclease has been assigned to histidine residue 12. This was accomplished by a direct comparison of the rate of tritium incorporation into position C-2 of histidine 12 of S-peptide (residues 1 to 20) derived from ribonuclease S, with the rates of deuterium exchange of the four histidine C-2 proton resonances of ribonuclease S under the same experimental conditions. The same assignment was obtained by a comparison of the NMR titration curves of ribonuclease S, the noncovalent complex of S-peptide and S-protein (residues 21 to 124) with the results for the recombined complex in which position C-2 of histidine 12 was fully deuterated. The second active site histidine resonance was assigned to histidine residue 119 by consideration of the NMR titration results fro carboxymethylated histidines and 1-carboxymethylhistidine 119 ribonuclease. This assignment is a reversal of that originally reported, and has important implications for the interpretation of NMR titration data of ribonuclease.
牛胰核糖核酸酶四个可滴定的组氨酸环C-2质子共振峰之一已被确定为组氨酸残基12。这是通过直接比较从核糖核酸酶S衍生的S-肽(残基1至20)中组氨酸12的C-2位掺入氚的速率,与在相同实验条件下核糖核酸酶S的四个组氨酸C-2质子共振峰的氘交换速率来实现的。通过比较核糖核酸酶S、S-肽与S-蛋白(残基21至124)的非共价复合物的NMR滴定曲线,与其中组氨酸12的C-2位完全氘化的重组复合物的结果,也得到了相同的归属。通过考虑羧甲基化组氨酸和1-羧甲基组氨酸119核糖核酸酶的NMR滴定结果,将第二个活性位点组氨酸共振峰确定为组氨酸残基119。这一归属与最初报道的相反,对核糖核酸酶NMR滴定数据的解释具有重要意义。