Measuring Protein Synthesis in Cultured Cells and Mouse Tissues Using the Non-radioactive SUnSET Assay

Abstract

Changes in protein synthesis occur under diverse physiological and pathological conditions. For example, translation can increase in response to growth signals or decrease in response to pathological states. Such changes have traditionally been measured by tracking the incorporation of radiolabeled amino acids. However, use of radioactivity is increasingly disfavored, and a simple and efficient puromycin-based, non-radioactive method called the SUnSET assay has gained popularity for measuring protein synthesis in diverse cell types and tissues. Here, we describe the principles, procedures, and troubleshooting steps for measuring protein synthesis using the SUnSET assay in cultured cells and mouse tissues. © 2020 Wiley Periodicals LLC

Basic Protocol 1: Measuring protein synthesis in cultured cells by western blotting

Support Protocol 1: Ponceau staining

Support Protocol 2: Testing the specificity of the anti-puromycin antibody

Basic Protocol 2: Measuring protein synthesis in cultured cells by immunofluorescence

Basic Protocol 3: Measuring protein synthesis in mouse tissues by western blotting