Leiden Institute of Chemistry, Gorlaeus Laboratories, Leiden University, Einsteinweg 55, 2333, CC, Leiden, The Netherlands.
Department of Physics, Huygens-Kamerlingh Onnes Laboratory, Leiden University, PO box 9504, 2300, RA, Leiden, The Netherlands.
Chemistry. 2020 Dec 18;26(71):17128-17133. doi: 10.1002/chem.202002743. Epub 2020 Nov 17.
The application of double electron-electron resonance (DEER) with site-directed spin labeling (SDSL) to measure distances in proteins and protein complexes in living cells puts rigorous restraints on the spin-label. The linkage and paramagnetic centers need to resist the reducing conditions of the cell. Rigid attachment of the probe to the protein improves precision of the measured distances. Here, three two-armed Gd complexes, Gd -CLaNP13a/b/c were synthesized. Rather than the disulfide linkage of most other CLaNP molecules, a thioether linkage was used to avoid reductive dissociation of the linker. The doubly Gd labeled N55C/V57C/K147C/T151C variants of T4Lysozyme were measured by 95 GHz DEER. The constructs were measured in vitro, in cell lysate and in Dictyostelium discoideum cells. Measured distances were 4.5 nm, consistent with results from paramagnetic NMR. A narrow distance distribution and typical modulation depth, also in cell, indicate complete and durable labeling and probe rigidity due to the dual attachment sites.
双电子-电子共振(DEER)与定点自旋标记(SDSL)在活细胞中测量蛋白质和蛋白质复合物中的距离的应用对自旋标记有严格的限制。连接物和顺磁中心需要抵抗细胞的还原条件。探针与蛋白质的刚性连接可提高测量距离的精度。在此,合成了三个双臂 Gd 配合物 Gd-CLaNP13a/b/c。与大多数其他 CLaNP 分子的二硫键连接不同,使用硫醚键连接以避免连接物的还原解离。通过 95GHz 的 DEER 测量 T4 溶菌酶的 N55C/V57C/K147C/T151C 双 Gd 标记变体。在体外、细胞裂解物和盘基网柄菌细胞中测量了这些构建体。测量的距离为 4.5nm,与顺磁 NMR 的结果一致。在细胞中也存在较窄的距离分布和典型的调制深度,这表明由于双连接点,标记完全且持久,并且探针具有刚性。