Skip to main content
Log in

Affinity labelling of yeast ribosomal peptidyl transferase

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

Using p-nitrophenylcarbamyl-phenylananyl-tRNA (PNPC-Phe-tRNA) and N-Iodoacetyl-phenylalanyl-tRNA as affinity labels we have attempted to identify the components of the aminoacyl-tRNA binding sites located in the vicinity of the peptidyl transferase centre of the yeast ribosome. Both Phe-tRNA derivatives bind to the ribosomal A-site in the presence of 20 mM Mg++ ion concentration and can be translocated to the ribosomal P-site in the presence of elongation factor. After the labels have been allowed to react covalently with ribosomes they were found associated with the large ribosomal subunit. Proteins L36, L43, L42, L29, L2, L17/18, L19/20 and proteins L26, L38, L22/23, L7/9, L4/6, L36, L11, L43, L39 were labelled in samples treated with PNPC-Phe-tRNA and N-Iodoacetyl-Phe-tRNA respectively. In contrast, when only the components of the ribosomal P-site were analysed by reacting the treated particles with puromycin fewer spots were labelled, corresponding to proteins L36 and L19/20 using PNPC-Phe-tRNA and proteins L4/6, L36, and L43 using N-Iodoacetyl-Phe-tRNA.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bakardjieva, A., Crichton, R.R.: Topography of Escherichia coli ribosomal proteins. The order of reactivity of thiol groups. Biochem. J. 143, 599–606 (1974)

    Google Scholar 

  • Barritault, D., Expert-Benzanzon, A., Guerin, M.F., Hayes, D.: The use of acetone precipitation in the isolation of ribosomal proteins. Europ. J. Biochem. 63, 131–135 (1976)

    Google Scholar 

  • Cantor, C.R., Pellegrini, M., Oen, H.: Affinity labeling techniques for examining functional sites of ribosomes. In: Ribosomes (M. Nomura, A. Tissieres and P. Lengyel, eds.), pp. 573–586. N.Y. Cold Spring Harbor Laboratory 1964

    Google Scholar 

  • Czernilofsky, A.P., Collatz, E., Gressner, A.M., Wool, I., Kuechler, E.: Identification of the tRNA-binding sites on rat liver ribosomes by affinity labeling. Molec. gen. Genet. 153, 231–235 (1977)

    Google Scholar 

  • Czernilofsky, A.P., Collatz, E., Stoffler, G., Kuechler, E.: Proteins at the tRNA binding sites of Escherichia coli ribosomes. Proc. nat. Acad. Sci. (Wash.) 71, 230–234 (1974)

    Google Scholar 

  • Czernilofsky, A.P., Kuechler, E.: Affinity label for the tRNA binding site on the Escherichia coli ribosomes. Biochim. biophys. Acta (Amst.) 272, 667–671 (1977)

    Google Scholar 

  • Diezel, W., Kopperschlager, G., Hofmann, E.: An improved procedure for protein staining in polyacrylamide gels with a new type of Coomassie brilliant blue. Analyt. Biochem. 48, 621–623 (1972)

    Google Scholar 

  • Gurd, F.N.R.: Carboxymethylation. Methods Enzymol. 11, 532–541 (1967)

    Google Scholar 

  • Hardy, S.J.S.: The stoichiometry of the ribosomal proteins of Escherichia coli. Molec. gen. Genet. 140, 253–274 (1975)

    Google Scholar 

  • Howard, G.A., Traut, R.R.: A modified two-dimensional gel system for the separation and radioautography of microgram amounts of ribosomal proteins. Methods Enzymol. 30, 526–539 (1974)

    Google Scholar 

  • Jiménez, A., Sánchez, L., Vázquez, D.: Simultaneous ribosomal resistance to trichodermin and anisomycin in Saccharomyces cerevisiae mutants. Biochim. biophys. Acta (Amst.) 383, 427–434 (1975)

    Google Scholar 

  • Kruiswijk, T., Planta, R.J.: Analysis of the protein composition of yeast ribosomal subunits by two-dimensional polyacrylamide gel electrophoresis. Mol. Biol. Reports 1, 409–415 (1974)

    Google Scholar 

  • Loening, U.E.: The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis. Biochem. J. 102, 251–257 (1967)

    Google Scholar 

  • Reyes, R., Vázquez, D., Ballesta, J.P.G.: Structure and function of ratliver ribosomes. Modification by 2-methoxy-5-nitrotropone treatment. Europ. J. Biochem. 67, 267–274 (1976a)

    Google Scholar 

  • Reyes, R., Vázquez, D., Ballesta, J.P.G.: Activities of nucleo-protein particles derived from rat liver ribosome. Biochim. biophys. Acta (Amst.) 435, 317–332 (1976b)

    Google Scholar 

  • Reyes, R., Vázquez, D., Ballesta, J.P.G.: Peptidyl transferase center of rat-liver ribosome cores. Europ. J. Biochem. 73, 25–31 (1977)

    Google Scholar 

  • Siler, J., Moldave, K.: Reactions of N-acetylphenylalanyl transfer RNA with rat liver ribosomes. Biochim. biophys. Acta (Amst.) 195, 130–137 (1969)

    Google Scholar 

  • Sopori, M., Pellegrini, M., Lengyel, P., Cantor, C.R.: Affinity labeling of Escherichia coli ribosomal proteins with analog of the natural initiator tRNA. Biochemistry 13, 5432–5439 (1974)

    Google Scholar 

  • Vázquez, D.: Inhibitors of protein synthesis. FEBS Letters 40, supplement, S63-S84 (1974)

    Google Scholar 

  • Yukioka, M., Hatayama, T., Morisawa, S.: Affinity labeling of the ribonucleic acid component adjacent to the peptidyl recognition center of peptidyl transferase in Escherichia coli ribosomes. Biochim. biophys. Acta (Amst.) 390, 192–208 (1975)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by H.G. Wittmann

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pérez-Gosálbez, M., Vázquez, D. & Ballesta, J.P.G. Affinity labelling of yeast ribosomal peptidyl transferase. Molec. Gen. Genet. 163, 29–34 (1978). https://doi.org/10.1007/BF00268961

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00268961

Keywords

Navigation