Literature DB >> 563404

The mechanism of killing of mouse fibroblasts by the amino acid analogue 5-fluorotryptophan.

M Taub.   

Abstract

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.

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Year:  1977        PMID: 563404     DOI: 10.1002/jcp.1040930204

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  3 in total

1.  Identification of the gene encoding the tryptophan synthase beta-subunit from Chlamydomonas reinhardtii.

Authors:  A L Palombella; S K Dutcher
Journal:  Plant Physiol       Date:  1998-06       Impact factor: 8.340

2.  5'-Nucleotidase activity in liver homogenates of rats treated with CCl4, colchicine, cycloheximide, emetine, ethanol, ethionine and 5-fluorotryptophan.

Authors:  C Agostini; M Secchi; D Venturelli
Journal:  Experientia       Date:  1980-09-15

3.  The pathophysiology of neurofibromatosis. I. Resistance in vitro to 3-nitrotyrosine as an expression of the mutation.

Authors:  V M Riccardi; V A Maragos
Journal:  In Vitro       Date:  1980-08
  3 in total

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