Taub M
J Cell Physiol. 1977 Nov;93(2):189-95. doi: 10.1002/jcp.1040930204.
The mechanism of killing of A9 fibroblasts by 5-fluorotryptophan has been studied. L-tryptophan competitively relieves the growth inhibition caused by 5FT. After incubation with 5FT, 3H-5FT was incorporated into protein, replacing tryptophan residues. During the initial hours of incubation with 5FT, a specific inhibition was observed of the incorporation of L-tryptophan into protein; later this inhibition was followed by a general inhibition of protein synthesis and cell division. However, nuclear division continued after cell division had ceased. While 5FT was observed to be incorporated into protein after a 1 hour period in MEM + 0.40 mM 5FT in A9, no 3H-5FT was incorporated into protein in a mutant isolated by its resistance to killingy by 5FT. These results support the hypothesis that cell death occurs due to malfunctioning proteins which contain 5FT residues.
已对5-氟色氨酸杀死A9成纤维细胞的机制进行了研究。L-色氨酸竞争性地缓解了5FT引起的生长抑制。用5FT孵育后,3H-5FT被掺入蛋白质中,取代了色氨酸残基。在用5FT孵育的最初几个小时内,观察到L-色氨酸掺入蛋白质受到特异性抑制;随后这种抑制之后是蛋白质合成和细胞分裂的普遍抑制。然而,在细胞分裂停止后核分裂仍在继续。虽然在含有0.40 mM 5FT的MEM中孵育1小时后观察到5FT被掺入A9细胞的蛋白质中,但在通过对5FT杀伤具有抗性而分离出的一个突变体中,没有3H-5FT被掺入蛋白质中。这些结果支持了这样的假说,即细胞死亡是由于含有5FT残基的蛋白质功能异常所致。