Development, validation, and application of the ribosome separation and reconstitution system for protein translation in vitro

  1. Natalia Shcherbik1
  1. 1Department of Cell Biology and Neuroscience, Rowan University, School of Osteopathic Medicine, Stratford, New Jersey 08084, USA
  2. 2Graduate School of Biomedical Sciences, Rowan University, Stratford, New Jersey 08084, USA
  1. Corresponding author: shcherna{at}rowan.edu

Abstract

Stress-induced molecular damage to ribosomes can impact protein synthesis in cells, but cell-based assays do not provide a clear way to distinguish the effects of ribosome damage from stress responses and damage to other parts of the translation machinery. Here we describe a detailed protocol for the separation of yeast ribosomes from other translational machinery constituents, followed by reconstitution of the translation mixture in vitro. This technique, which we refer to as ribosome separation and reconstitution (RSR), allows chemical modifications of yeast ribosomes without compromising other key translational components. In addition to the characterization of stress-induced ribosome damage, RSR can be applied to a broad range of experimental problems in studies of yeast translation.

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Footnotes

  • Received June 3, 2021.
  • Accepted August 18, 2021.

This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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