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Gd3+ - Gd3+ distances exceeding 3 nm determined by very high frequency continuous wave electron paramagnetic resonance

机译:Gd3 +-Gd3 +的距离超过3 nm由超高频连续波电子顺磁共振确定

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摘要

Electron paramagnetic resonance spectroscopy in combination with site-directed spin-labeling is a very powerful tool for elucidating the structure and organization of biomolecules. Gd3+ complexes have recently emerged as a new class of spin labels for distance determination by pulsed EPR spectroscopy at Q- and W-band. We present CW EPR measurements at 240 GHz (8.6 Tesla) on a series of Gd-rulers of the type Gd-PyMTA—spacer—Gd-PyMTA, with Gd-Gd distances ranging from 1.2 nm to 4.3 nm. CW EPR measurements of these Gd-rulers show that significant dipolar broadening of the central |−1/2〉 → |1/2〉 transition occurs at 30 K for Gd-Gd distances up to ~ 3.4 nm with Gd-PyMTA as the spin label. This represents a significant extension for distances accessible by CW EPR, as nitroxide-based spin labels at X-band frequencies can typically only access distances up to ~ 2 nm. We show that this broadening persists at biologically relevant temperatures above 200 K, and that this method is further extendable up to room temperature by immobilizing the sample in glassy trehalose. We show that the peak-to-peak broadening of the central transition follows the expected 1/r3 dependence for the electron-electron dipolar interaction, from cryogenic temperatures up to room temperature. A simple procedure for simulating the dependence of the lineshape on interspin distance is presented, in which the broadening of the central transition is modeled as an S = 1/2 spin whose CW EPR lineshape is broadened through electron-electron dipolar interactions with a neighboring S = 7/2 spin.
机译:电子顺磁共振波谱结合定点自旋标记是阐明生物分子的结构和组织的非常强大的工具。 Gd 3 + 配合物最近成为一类新型的自旋标记,可通过脉冲EPR光谱在Q和W波段确定距离。我们介绍了一系列Gd-PyMTA-垫片-Gd-PyMTA类型的Gd尺在240 GHz(8.6特斯拉)上的连续EPR测量值,Gd-Gd距离范围为1.2 nm至4.3 nm。这些Gd规则的CW EPR测量表明,当Gd-Gy-Gd距离高达〜3.4 nm时,以Gd-PyMTA自旋,中心| −1 / 2〉→| 1 / 2〉跃迁发生了显着的偶极展宽标签。这代表了CW EPR可访问距离的显着扩展,因为X波段频率上基于氮氧化物的自旋标签通常只能访问约2 nm的距离。我们表明,这种扩展在高于200 K的生物学相关温度下持续存在,并且通过将样品固定在玻璃状海藻糖中,该方法可以进一步扩展到室温。我们表明,从低温到室温,中心跃迁的峰到峰展宽遵循电子/电子偶极相互作用的预期1 / r 3 依赖性。提出了一种简单的模拟线形对自旋间距离的依赖性的程序,其中,中心跃迁的展宽建模为S = 1/2自旋,其CW EPR线形通过与相邻S的电子-电子偶极相互作用而展宽= 7/2旋转。

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