Davis D G, Perlman M E, London R E
Laboratory of Molecular Biophysics, NIEHS, Research Triangle Park, North Carolina 27709.
J Magn Reson B. 1994 Jul;104(3):266-75. doi: 10.1006/jmrb.1994.1084.
The unimolecular dissociation rate constant, k-1, for the inhibitor-enzyme complex tubercidin-Escherichia coli purine nucleoside phosphorylase (PNPase) has been determined directly via two related 1H NMR methods for studying exchange-mediated transverse relaxation. One method involves measurements of the decay rate, 1/T1 rho, of spin-locked magnetization in the rotating frame as a function of the strength of the spin-locking field, omega SL. The second method involves measurements of the Carr-Purcell-Meiboom-Gill (CPMG) spin-echo decay rate, 1/TCPMG2, as a function of the repetition rate, 1/tcp, of the refocusing pulses. Expressions describing the dependence of TCPMG2 as a function of 1/tcp and k-1 have been previously derived with sufficient generality to include the two-site inhibitor-enzyme exchange case. Existing expressions for T1 rho as a function of kex and omega SL, however, had to be reformulated to take into account differences between Tb2 and Tb1 for the bound form of the inhibitor as well as offset corrections important at low values of omega SL. A new expression for exchange-mediated T1 rho has been derived to take these factors into account and is shown to provide a more accurate description of observed T1 rho data than previous models. Numerical analysis of relaxation rates, measured independently by either the rotating-frame or the spin-echo method for the H1' and H2 protons of tubercidin at different inhibitor:enzyme ratios, yields comparable values for k-1 of 2400 (+/- 350) and 900 (+/- 80) s-1 at 20 and 10 degrees C, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
已通过两种相关的1H NMR方法直接测定了抑制剂 - 酶复合物结核菌素 - 大肠杆菌嘌呤核苷磷酸化酶(PNPase)的单分子解离速率常数k-1,以研究交换介导的横向弛豫。一种方法涉及测量旋转框架中自旋锁定磁化强度的衰减率1/T1ρ作为自旋锁定场强度ωSL的函数。第二种方法涉及测量Carr-Purcell-Meiboom-Gill(CPMG)自旋回波衰减率1/TCPMG2作为重聚焦脉冲重复率1/tcp的函数。先前已经推导出描述TCPMG2作为1/tcp和k-1函数的依赖关系的表达式,其普遍性足以包括双位点抑制剂 - 酶交换情况。然而,必须重新制定T1ρ作为kex和ωSL函数的现有表达式,以考虑抑制剂结合形式的Tb2和Tb1之间的差异以及在低ωSL值时重要的偏移校正。已经推导出一个新的交换介导的T1ρ表达式以考虑这些因素,并且显示出比以前的模型更准确地描述观察到的T1ρ数据。通过旋转框架或自旋回波方法独立测量不同抑制剂:酶比例下结核菌素H1'和H2质子的弛豫率的数值分析,在20和10摄氏度下分别得到k-1的可比数值,分别为2400(±350)和900(±80)s-1。(摘要截断于250字)