Johnson M E
Biochemistry. 1979 Jan 23;18(2):378-84. doi: 10.1021/bi00569a023.
Practical techniques are demonstrated for determining rotational correlation times of macromolecules from the first harmonic absorption electron spin reasonance spectra of tightly bound spin labels. The techniques are developed to compensate for such nonideal conditions as residual label motion, temperature dependence of rigid limit spectral parameters, and the presence of inhomogeneous line broadening. These effects are all shown to be of importance in monitoring the rotational motion of carbonmonoxyhemoglobin which is spin labeled with the tightly bound nitroxide label, 4-maleimido-2,2,6,6-tetramethylpiperidinyl-1-oxy. Spin-label interactions with other paramagnetic agents are also shown to produce spectral changes which are qualitatively similar to, but quantitatively different from, those resulting from increases in the rate of rotational motion.
本文展示了从紧密结合的自旋标记的一次谐波吸收电子自旋共振光谱中确定大分子旋转相关时间的实用技术。这些技术是为补偿诸如残留标记运动、刚性极限光谱参数的温度依赖性以及非均匀线宽展宽等非理想条件而开发的。在监测用紧密结合的氮氧化物标记4-马来酰亚胺-2,2,6,6-四甲基哌啶基-1-氧基自旋标记的碳氧血红蛋白的旋转运动时,所有这些效应都显示出其重要性。自旋标记与其他顺磁剂的相互作用也显示会产生光谱变化,这些变化在定性上与旋转运动速率增加所导致的变化相似,但在定量上不同。