Department of Chemistry and Chemical Biology and ACERT, Cornell University, Ithaca, NY 14853, United States.
J Magn Reson. 2012 Mar;216:69-77. doi: 10.1016/j.jmr.2012.01.004. Epub 2012 Jan 24.
Pulsed dipolar ESR spectroscopy, DEER and DQC, require frozen samples. An important issue in the biological application of this technique is how the freezing rate and concentration of cryoprotectant could possibly affect the conformation of biomacromolecule and/or spin-label. We studied in detail the effect of these experimental variables on the distance distributions obtained by DEER from a series of doubly spin-labeled T4 lysozyme mutants. We found that the rate of sample freezing affects mainly the ensemble of spin-label rotamers, but the distance maxima remain essentially unchanged. This suggests that proteins frozen in a regular manner in liquid nitrogen faithfully maintain the distance-dependent structural properties in solution. We compared the results from rapidly freeze-quenched (≤100 μs) samples to those from commonly shock-frozen (slow freeze, 1 s or longer) samples. For all the mutants studied we obtained inter-spin distance distributions, which were broader for rapidly frozen samples than for slowly frozen ones. We infer that rapid freezing trapped a larger ensemble of spin label rotamers; whereas, on the time-scale of slower freezing the protein and spin-label achieve a population showing fewer low-energy conformers. We used glycerol as a cryoprotectant in concentrations of 10% and 30% by weight. With 10% glycerol and slow freezing, we observed an increased slope of background signals, which in DEER is related to increased local spin concentration, in this case due to insufficient solvent vitrification, and therefore protein aggregation. This effect was considerably suppressed in slowly frozen samples containing 30% glycerol and rapidly frozen samples containing 10% glycerol. The assignment of bimodal distributions to tether rotamers as opposed to protein conformations is aided by comparing results using MTSL and 4-Bromo MTSL spin-labels. The latter usually produce narrower distance distributions.
脉冲双共振电子自旋共振波谱学、DEER 和 DQC 需要冷冻样品。该技术在生物应用中的一个重要问题是,冷冻速率和冷冻保护剂浓度如何可能影响生物大分子的构象和/或自旋标记。我们详细研究了这些实验变量对一系列双自旋标记 T4 溶菌酶突变体的 DEER 获得的距离分布的影响。我们发现,样品冷冻速率主要影响自旋标记旋转异构体的总体,但距离最大值基本不变。这表明以规则方式在液氮中冷冻的蛋白质忠实保持溶液中距离相关的结构特性。我们将快速冷冻(≤100 μs)样品的结果与通常冲击冷冻(慢速冷冻,1 s 或更长时间)样品的结果进行了比较。对于所有研究的突变体,我们获得了自旋间距分布,对于快速冷冻的样品,其分布比慢速冷冻的样品更宽。我们推断,快速冷冻捕获了更大的自旋标记旋转异构体总体;而在较慢冷冻的时间尺度上,蛋白质和自旋标记达到了表现出较少低能量构象的种群。我们使用甘油作为冷冻保护剂,浓度分别为 10%和 30%(按重量计)。使用 10%甘油和慢速冷冻,我们观察到背景信号斜率增加,在 DEER 中,这与局部自旋浓度增加有关,在这种情况下,由于溶剂玻璃化不足,导致蛋白质聚集。在含有 30%甘油的慢速冷冻样品和含有 10%甘油的快速冷冻样品中,这种效应得到了极大的抑制。通过比较使用 MTSL 和 4-溴 MTSL 自旋标记的结果,有助于将双模态分布分配给系绳旋转异构体,而不是蛋白质构象。后者通常产生更窄的距离分布。