The acidic ribosomal stalk proteins are not required for the highly specific inactivation exerted by α-sarcin of the eukaryotic ribosome

Biochemistry. 2014 Mar 18;53(10):1545-7. doi: 10.1021/bi401470u. Epub 2014 Mar 4.

Abstract

The ribosomal sarcin/ricin loop (SRL) is the target of ribosome-inactivating proteins like the N-glycosidase ricin and the fungal ribotoxin α-sarcin. The eukaryotic ribosomal stalk directly interacts with several members of the N-glycosidase family, favoring their disruption of the SRL. Here we tested this hypothesis for the ribotoxin α-sarcin. Experiments with isolated ribosomes, cell-free translation systems, and viability assays with Saccharomyces cerevisiae strains defective in acidic stalk proteins showed that the inactivation exerted by α-sarcin is independent of the composition of the ribosomal stalk. Therefore, α-sarcin, with the same ribosomal target as ricin, seems to access the SRL by a different pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoribonucleases / metabolism*
  • Fungal Proteins / metabolism*
  • Protein Biosynthesis*
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / metabolism*
  • Ribosomes / genetics
  • Ribosomes / metabolism*
  • Ricin / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • Fungal Proteins
  • Ribosomal Proteins
  • Saccharomyces cerevisiae Proteins
  • alpha-sarcin
  • Ricin
  • Endoribonucleases