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The site of action of inhibitors of initiation of protein synthesis in reticulocytes
- Source :
- Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis. 277:188-197
- Publication Year :
- 1972
- Publisher :
- Elsevier BV, 1972.
-
Abstract
- The inhibitors of initiation pactamycin, cycloheximide, NaF, aurintricarboxylic acid and pederine have been found to inhibit the reaction of initiator tRNA with puromycin, as measured by the formation of N- formyl [ 35 S]methionylpuromycin . None of these inhibitors, with the exception of aurintricarboxylic acid, inhibits, however, the binding of the initiator tRNA to ribosomes, as measured by the binding of [35S]Met-tRNAf to unwashed or washed ribosomes. This binding is stimulated by the codon AUG; the stimulatory activity of this trinucleotide decreases with time even when ribosomes are kept at 0°C. The ribosomal components that bind initiator tRNA have been analyzed by sucrose gradient centrifugation; Met-tRNAf is bound by polyribosomes, 80-S ribosomes and 40-S ribosomal subunit. Those compounds that inhibit elongation as well as initiation, like cycloheximide, pactamycin and pederine, interfere presumably with a biochemical step common to both processes.
- Subjects :
- Peptide Biosynthesis
Reticulocytes
Cyclohexanecarboxylic Acids
Formates
Polynucleotides
In Vitro Techniques
Cycloheximide
Biology
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Ribosome
Potassium Chloride
Fluorides
chemistry.chemical_compound
Methionine
RNA, Transfer
Polysome
Sulfur Isotopes
Aurintricarboxylic acid
Centrifugation, Density Gradient
Protein biosynthesis
Animals
Peptide Chain Initiation, Translational
Pyrans
Antibiotics, Antineoplastic
Pactamycin
Amides
Kinetics
chemistry
Biochemistry
Puromycin
Protein Biosynthesis
Rabbits
Eukaryotic Ribosome
Ribosomes
Subjects
Details
- ISSN :
- 00052787
- Volume :
- 277
- Database :
- OpenAIRE
- Journal :
- Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis
- Accession number :
- edsair.doi.dedup.....4ace3609b189809eae04323d0d1dbd67
- Full Text :
- https://doi.org/10.1016/0005-2787(72)90365-6