Direct conversion of EPR dipolar time evolution data to distance distributions

被引:197
作者
Jeschke, G [1 ]
Koch, A [1 ]
Jonas, U [1 ]
Godt, A [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55028 Mainz, Germany
关键词
pulse EPR; solid state; distance measurements; nitroxide; radial distribution function;
D O I
10.1006/jmre.2001.2498
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Shallow electron spin echo envelope modulations due to dipole-dipole couplings between electron spins provide information on the radial distribution function of the spins in disordered systems while angular correlations between spin pairs are negligible. Under these conditions and in the absence of orientational selection, the dipolar time evolution data can be quantitatively simulated for arbitrary radial distribution functions by shell factorization, i.e., by performing the orientational average separately for thin spherical shells and multiplying the signals of all the shells. For distances below 5 nm, a linear superposition of the signals of the shells is sufficient. The dipolar time evolution data can be separated into this linear contribution and a nonlinear background. The linear contribution can then be converted directly to a radial distribution function. For a series of shape-persistent and flexible biradicals with end-to-end distances between 2 and 5 nm, shell factorization and direct conversion of the data are in good agreement with each other and with force-field computations of the end-to-end distances. The neglect of orientation selection does not cause significant distortions of the determined distance distributions. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:72 / 82
页数:11
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