Juul M E, Dornish J M, Juul N O, Pettersen E O, Oftebro R
Department of Tissue Culture, Norwegian Radium Hospital, Montebello, Oslo.
Mol Cell Biochem. 1990 Aug 10;96(2):117-26. doi: 10.1007/BF00420903.
Accumulation of tubulin as compared with the accumulation of total cellular protein in human NHIK 3025 cells treated with the sulfone 2-(2-thenyl)sulfonyl-5-bromopyrimidine (NY 4137) and the sulfoxide 2-(2-thenyl)sulfinyl-5-bromopyrimidine (NY 4138), two mitotic inhibitors, were investigated by two-parametric flow cytometry. Following a 4 h treatment with NY 4137 tubulin accumulation is inhibited while total protein continues to accumulate. After treatment for 4 h with NY 4138 the accumulation of total protein is approximately constant, while the accumulation of tubulin is reduced although not to the same degree as that found for NY 4137-treated cells. In addition, the percentage tubulin SH-groups (6.89 +/- 0.14) remaining after treatment of purified rat brain tubulin with NY 4137 or NY 4138 was determined. Treatment with 0.0125 mM NY 4137 reduced the number of tubulin SH-groups detectable with dithiobis benzoate or from 6.89 +/- 0.14 before treatment to about 4 after treatment. However, practically all SH-groups of tubulin remain detectable following treatment with the same concentration of NY 4138. From the results described in this report we infer that NY 4137 binds to tubulin SH-groups and that inhibition of tubulin accumulation follows as a secondary effect.
通过双参数流式细胞术研究了在人NHIK 3025细胞中,用两种有丝分裂抑制剂砜类化合物2-(2-噻吩基)磺酰基-5-溴嘧啶(NY 4137)和亚砜类化合物2-(2-噻吩基)亚磺酰基-5-溴嘧啶(NY 4138)处理后,微管蛋白的积累与总细胞蛋白积累的情况。用NY 4137处理4小时后,微管蛋白的积累受到抑制,而总蛋白继续积累。用NY 4138处理4小时后,总蛋白的积累大致保持恒定,而微管蛋白的积累减少,尽管减少程度不如用NY 4137处理的细胞。此外,还测定了用NY 4137或NY 4138处理纯化的大鼠脑微管蛋白后,剩余的微管蛋白SH基团的百分比(6.89±0.14)。用0.0125 mM NY 4137处理后,用二硫代双苯甲酸可检测到的微管蛋白SH基团数量从处理前的6.89±0.14减少到处理后的约4个。然而,在用相同浓度的NY 4138处理后,微管蛋白的几乎所有SH基团仍可检测到。根据本报告所述结果,我们推断NY 4137与微管蛋白SH基团结合,微管蛋白积累的抑制是随之产生的次要效应。