Studies on the Accessability of Ribosomes to Inactivation by the Toxic Lectins Abrin and Ricin
- 1 April 1977
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 74 (2), 209-215
- https://doi.org/10.1111/j.1432-1033.1977.tb11383.x
Abstract
The rate of protein synthesis in HeLa cells was measured at various periods of time after addition of abrin and ricin to the medium and compared with the concurrent ability of the isolated ribosomes to support poly(U)-stimulated synthesis of polyphenylalanine in a cell-free system. The endogenous synthesis in unfractionated cell-free systems from HeLa cells and rabbit reticulocytes was compared with the ability of the isolated ribosomes to support poly(U)-stimulated polymerization of phenylalanine. In the intact cells and the unfractionated cell-free systems protein synthesis decreased progressively with the time after addition of toxins or toxin A chains. The ability of the isolated ribosomes to support polyphenylalanine synthesis was only moderately reduced initially and then remained constant or even increased. The activity of isolated monosomes decreased progressively with time after addition of toxin A chain, whereas polysomes were only inactivated and the extent of inactivation varied from one experiment to another. The inactivation of one or a few ribosomes per polysome stops the translation of mRNA. It is suggested that the intact ribosomes thus trapped are inaccessible to the toxins and that the isolation of polysomes results in release of functionally intact ribosomes capable of supporting poly(U)-directed polymerization of phenylalanine.This publication has 25 references indexed in Scilit:
- Site of action of ricin on the ribosomeBiochemistry, 1976
- The Binding of Tritiated Elongation‐Factors 1 and 2 to Ribosomes from Krebs II Mouse Ascites‐Tumor CellsEuropean Journal of Biochemistry, 1976
- Cell free system from HeLa cells active in initiation of protein synthesisBiochemistry, 1975
- Effects of Ricin on the Ribosomal Sites Involved in the Interaction of the Elongation FactorsEuropean Journal of Biochemistry, 1975
- Available sulphydryl groups of mammalian ribosomes in different functional statesJournal of Molecular Biology, 1974
- Different biological properties of the two constituent peptide chains of ricin a toxic protein inhibiting protein synthesisBiochemistry, 1973
- Isolation and Properties of Abrin: a Toxic Protein Inhibiting Protein SynthesisEuropean Journal of Biochemistry, 1973
- Ricin — a potent inhibitor of protein synthesisFEBS Letters, 1972
- Colicin E3-directed changes in ribosome function and polyribosome metabolism in Escherichia coli K12Journal of Molecular Biology, 1970
- Interaction of colicins with bacterial cellsJournal of Molecular Biology, 1967