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Improving real-time measurement of H/D exchange using a FTIR biospectroscopic probe

机译:使用FTIR生物光谱探针改善H / D交换的实时测量

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摘要

We describe the improvement of a novel approach to investigating hydrogen/deuterium (H/D) exchange kinetics in biomolecules using transmission infrared spectroscopy. The method makes use of a Fourier transform infrared spectrometer coupled with a microdialysis flow cell to determine exchange rates of labile hydrogens. With this cell system, the monitoring of exchange reactions has been studied here as a function of some cell characteristics such as: (a) dialysis membrane surface contacting both the H2O and D2O compartments; (b) molecular cutoff of dialysis membrane; and (c) distance between the cell-filling holes. The best improvement has been obtained by increasing the dialysis membrane surface followed by increase of molecular cutoff. However, not significant differences were found using various distances between filling holes. The fastest exchange rate which can be measured with the cell system used here is found to be k = 0.41 +/- 0.02 min(-1), that is, about threefold greater than the one got in a previous work. This microdialysis flow cell has been used here for the study of H/D exchange in nucleic acids with subsequent structural analysis by 2D correlation spectroscopy.
机译:我们描述了一种新型方法的改进,该方法用于研究使用透射红外光谱技术的生物分子中的氢/氘(H / D)交换动力学。该方法利用傅立叶变换红外光谱仪与微透析流通池相结合来确定不稳定氢的交换速率。利用这种细胞系统,在这里已经研究了交换反应的监测与某些细胞特征的关系,例如:(a)接触H2O和D2O隔室的透析膜表面; (b)透析膜的分子截止; (c)细胞填充孔之间的距离。通过增加透析膜​​的表面,然后增加分子的截留率,可以得到最好的改善。然而,使用填充孔之间的各种距离并没有发现显着差异。可以用此处使用的细胞系统测量的最快交换速率为k = 0.41 +/- 0.02 min(-1),即比以前的工作中的交换速率大三倍。这种微透析流动池已用于核酸的H / D交换研究,随后通过2D相关光谱进行结构分析。

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