Sudmeier James L, Bradshaw Elizabeth M, Haddad Kristin E Coffman, Day Regina M, Thalhauser Craig J, Bullock Peter A, Bachovchin William W
Department of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Am Chem Soc. 2003 Jul 16;125(28):8430-1. doi: 10.1021/ja034072c.
If the 13Cdelta2 chemical shift of neutral ("high pH") histidine is >122 ppm, primarily Ndelta1-H tautomer (2) is indicated; if it is <122 ppm, primarily Nepsilon2-H tautomer (1) is indicated. His resonances from the catalytic triad of active serine proteases, for example, are readily distinguished from those of denatured enzyme. The 13Cdelta2 chemical shifts increased by 6.2 ppm for the catalytic histidines in both alpha-lytic protease and subtilisin BPN' in raising the pH from that of imidazolium cation to that of tautomer 2. This tautomer identification method is easy to implement, requiring only bioincorporation of [U-13C] (or the more readily available [U-13C,15N])-histidine. Standard 1H/13C correlation HMQC or HSQC NMR pulse programs then yield the 13Cdelta2 chemical shifts with the benefit of high 1H sensitivity. Because of large one-bond spin-couplings (1JCH approximately 200 Hz), the method should extend to proteins having large 1H and 13C line widths, including very high molecular weights.
如果中性(“高pH值”)组氨酸的13Cδ2化学位移>122 ppm,则表明主要是Nδ1-H互变异构体(2);如果<122 ppm,则表明主要是Nε2-H互变异构体(1)。例如,活性丝氨酸蛋白酶催化三联体中的组氨酸共振很容易与变性酶的共振区分开来。在将α-裂解蛋白酶和枯草杆菌蛋白酶BPN'中的催化组氨酸的pH值从咪唑阳离子的pH值提高到互变异构体2的pH值时,13Cδ2化学位移增加了6.2 ppm。这种互变异构体鉴定方法易于实施,只需要生物掺入[U-13C](或更容易获得的[U-13C,15N])-组氨酸。然后,标准的1H/13C相关HMQC或HSQC NMR脉冲程序可在具有高1H灵敏度的情况下得出13Cδ2化学位移。由于存在较大的一键自旋耦合(1JCH约为200 Hz),该方法应适用于具有较大1H和13C线宽的蛋白质,包括非常高的分子量。