Literature DB >> 1016237

Re-activation of the peptidyltransferase centre of rabbit reticulocyte ribosomes after inactivation by exposure to low concentrations of magnesium ion.

R A Cox, P Greenwell, W Hirst.   

Abstract

1. The larger subrivosomal particles of rabbit reticulocytes retained full activity in the puromycin reaction and in poly(U)-directed polyphenylalanine synthesis after 4h at 0 degrees C when buffered 0.5M-NH4Cl/10-30mM-MgCl2 was the solvent. 2. Activity in the puromycin reaction was diminished to approx 10% after 15-30 min at 0 degrees C when the concentration of MgCl2 was lowered to 2mM. 3. Activity was not restored when the concentration of MgCl2 was raised from 2mM to 10-30 mM at 0 degrees C. However, activity was recovered as measured by both assay systems when the ribosome fraction was heated to 37 degrees C at the higher concentrations of MgCl2. 4. Recovery of activity was noted during the course of the polyphenylalanine synthesis in 50 mM-KCl/5mM-MgCl2/25mM-Tris/HCl, pH 7.6, at 37 degrees C. Re-activation was slow at 20 degrees C and below. 5. No more than about 5% of the protein moiety of the subparticle was lost in 0.5M-NH4Cl on decreasing MgCl2 concentration from 10mM to 2mM. No proteins were detected in the supernatant fractions by gel electrophoresis after ribosomes were separated by differential centrifugation. The supernatant fraction was not essential for the recovery of activity. However, at higher (e.g. 1M) concentrations of NH4Cl, proteins were split from the subparticle. 6. The loss and regain of activity found on lowering and restoring the concentration of MgCl2 at 0.5M-NH4Cl appears to arise from a conformational change that does not seem to be associated with a loss and regain of particular proteins. 7. A 2% decrease in E260 was noticed when the concentration of Mg2+ was restored, and the change in the spectrum indicated a net increase of approx. 100A-U base-pairs per subribosomal particle. 8. When the concentration of Mg2+ was restored, S20,W of the subparticle remained at 52+/- 1S until the sample was incubated at 37 degrees C when S20,W increased to 56 +/- 1S compared with the value of 58 +/- 1S for the subparticle as originally isolated.

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Year:  1976        PMID: 1016237      PMCID: PMC1164268          DOI: 10.1042/bj1600521

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  30 in total

1.  Studies on ribosomes from reticulocytes.

Authors:  P O TS'O; J VINOGRAD
Journal:  Biochim Biophys Acta       Date:  1961-04-29

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

3.  Separation and radioautography of microgram quantities of ribosomal proteins by two-dimensional polyacrylamide gel electrophoresis.

Authors:  G A Howard; R R Traut
Journal:  FEBS Lett       Date:  1973-01-15       Impact factor: 4.124

4.  The involvement of 5S RNA in the binding of tRNA to ribosomes.

Authors:  V A Erdmann; M Sprinzl; O Pongs
Journal:  Biochem Biophys Res Commun       Date:  1973-10-01       Impact factor: 3.575

5.  Affinity labelling of 23-S ribosomal RNA in the active centre of Escherichia coli peptidyl transferase.

Authors:  P Greenwell; R J Harris; R H Symons
Journal:  Eur J Biochem       Date:  1974-12-02

6.  Characterization of the peptidyltransferase reaction catalyzed by rat liver 60S ribosomal subunits.

Authors:  H A Thompson; K Moldave
Journal:  Biochemistry       Date:  1974-03-26       Impact factor: 3.162

7.  Microdetermination of protein not affected by the presence of various buffers, sucrose, ATP, and eluates from polysaccharide derivatives.

Authors:  T Nakao; M Nakao; F Nagai
Journal:  Anal Biochem       Date:  1973-10       Impact factor: 3.365

8.  Studies of the RNA and protein moieties of the larger subribosomal particle of rabbit reticulocytes.

Authors:  E Godwin; R A Cox; P Huvos
Journal:  Acta Biol Med Ger       Date:  1974

9.  Reassembly of the peptidyltransferase centre of larger subparticles of rabbit reticulocyte ribosomes from a core-particle and split-protein fraction.

Authors:  R A Cox; P Greenwell
Journal:  Biochem J       Date:  1976-12-15       Impact factor: 3.857

10.  A study of the influence of magnesium ions on the conformation of ribosomal ribonucleic acid and on the stability of the larger subribosomal particle of rabbit reticulocytes.

Authors:  R A Cox; W Hirst
Journal:  Biochem J       Date:  1976-12-15       Impact factor: 3.857

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  6 in total

1.  Resistance of the peptidyltransferase centre of rabbit ribosomes to attack by nucleases and proteinases.

Authors:  R A Cox; S Kotecha
Journal:  Biochem J       Date:  1980-07-15       Impact factor: 3.857

2.  Reassembly of the peptidyltransferase centre of larger subparticles of rabbit reticulocyte ribosomes from a core-particle and split-protein fraction.

Authors:  R A Cox; P Greenwell
Journal:  Biochem J       Date:  1976-12-15       Impact factor: 3.857

3.  A study of the influence of magnesium ions on the conformation of ribosomal ribonucleic acid and on the stability of the larger subribosomal particle of rabbit reticulocytes.

Authors:  R A Cox; W Hirst
Journal:  Biochem J       Date:  1976-12-15       Impact factor: 3.857

4.  Distribution of sequences common to the 25--28S-ribonucleic acid genes of Xenopus laevis and Neurospora crassa.

Authors:  R A Cox; R D Thompson
Journal:  Biochem J       Date:  1980-04-01       Impact factor: 3.857

5.  Protein synthesis by hybrid ribosomes reconstructed from rabbit reticulocyte ribosomal core-particles and amphibian or fungal split-proteins.

Authors:  R A Cox; P Greenwell
Journal:  Biochem J       Date:  1980-03-15       Impact factor: 3.857

6.  Reconstruction of the smaller subparticle of rabbit ribosomes from core-particle and split-protein fractions.

Authors:  R A Cox
Journal:  Biochem J       Date:  1981-03-15       Impact factor: 3.857

  6 in total

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