García A E, Krumhansl J A, Frauenfelder H
Theoretical Biology and Biophysics Group, Los Alamos National Laboratory, New Mexico 87545, USA.
Proteins. 1997 Oct;29(2):153-60.
Debye and Waller showed how to adjust scattering intensities in diffraction experiments for harmonic motions of atoms about an average, static reference configuration. However, many motions, particularly in biological molecules as compared to simple crystals, are far from harmonic. We show how, using a variety of simple anharmonic, multiconformational models, it is possible to construct a variety of Generalized Debye-Waller Factors, and understand their meaning. A central result for these cases is that, in principle, intensity factors cannot be obtained from true total mean square displacements of the atoms. We make the distinction between the intensity factors for unimodal quasiharmonic motions and those for the anharmonic, multimodal (valley hopping) motions. Only the former affect the conventional B factors.
德拜和瓦勒展示了如何在衍射实验中针对原子围绕平均静态参考构型的简谐运动来调整散射强度。然而,许多运动,特别是与简单晶体相比的生物分子中的运动,远非简谐运动。我们展示了如何使用各种简单的非简谐、多构象模型来构建各种广义德拜 - 瓦勒因子,并理解它们的含义。这些情况的一个核心结果是,原则上强度因子不能从原子的真实总均方位移中获得。我们区分了单峰准简谐运动的强度因子和非简谐、多峰(谷跳跃)运动的强度因子。只有前者会影响传统的B因子。