Sutoo D, Akiyama K, Fujii N, Matsushita K
Biochim Biophys Acta. 1986 Sep 5;873(1):156-60. doi: 10.1016/0167-4838(86)90203-7.
The effect of W-7 (N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide), a calmodulin antagonist, on the structure of calmodulin was studied with 400 MHz H-NMR. W-7 affected the calcium-induced conformational change of calmodulin in several resonances. One resonant peak was assigned to the His-107 H2 proton. The other peaks were seen in the area of the methionine methyl group (around 2 ppm) and the high-field methyl group (0-1 ppm), these peaks cannot be assigned. The modifying effect of W-7 on the methyl-group resonances of calmodulin fully bound with Ca2+ was similar to that of trifluoperazine. However, the effect on the His-107 H2 proton was unique to W-7.
用400兆赫的氢核磁共振研究了钙调蛋白拮抗剂W-7(N-(6-氨基己基)-5-氯-1-萘磺酰胺)对钙调蛋白结构的影响。W-7在几个共振峰处影响钙诱导的钙调蛋白构象变化。一个共振峰归属于组氨酸-107的H2质子。其他峰出现在甲硫氨酸甲基区域(约2 ppm)和高场甲基区域(0 - 1 ppm),这些峰无法归属。W-7对与Ca2+完全结合的钙调蛋白甲基基团共振的修饰作用与三氟拉嗪相似。然而,对组氨酸-107 H2质子的影响是W-7独有的。