Pintacuda Guido, Otting Gottfried
Department of Medical Biochemistry and Biophysics, Karolinska Institute, Tomtebodavägen 6, S-171 77 Stockholm, Sweden.
J Am Chem Soc. 2002 Jan 23;124(3):372-3. doi: 10.1021/ja016985h.
Gd-diethylenetriamine pentaacetic acid-bismethylamide, Gd(DTPA-BMA), is shown to be a reagent suitable for the identification of protein surfaces. Compared to the conventionally used spin-label TEMPOL, Gd(DTPA-BMA) is a stronger relaxation agent, requiring lesser concentrations to achieve the same paramagnetic relaxation enhancement of solvent-exposed protein protons. It is also less hydrophobic and therefore less prone to specific binding to proteins. Relaxation enhancements predicted by a second-sphere interaction model correlated with experimental data recorded with ubiquitin, while the correlation with corresponding data recorded with TEMPOL was poor.
钆-二乙三胺五乙酸双甲酰胺(Gd(DTPA-BMA))被证明是一种适用于识别蛋白质表面的试剂。与传统使用的自旋标记物TEMPOL相比,Gd(DTPA-BMA)是一种更强的弛豫剂,达到相同的溶剂暴露蛋白质质子顺磁弛豫增强所需的浓度更低。它的疏水性也更低,因此与蛋白质特异性结合的倾向更小。由第二球体相互作用模型预测的弛豫增强与用泛素记录的实验数据相关,而与用TEMPOL记录的相应数据的相关性较差。