Author:
Capece Mark C.,Kornberg Guy L.,Petrov Alexey,Puglisi Joseph D.
Abstract
A high-throughput assay for real-time measurement of translation rates in cell-free protein synthesis (SNAP assay) is described. The SNAP assay enables quantitative, real-time measurement of overall translation rates in vitro via the synthesis of O6-alkylguanine DNA O6-alkyltransferase (SNAP). SNAP production is continuously detected by fluorescence produced by the reaction of SNAP with a range of quenched fluorogenic substrates. The capabilities of the assay are exemplified by measurements of the activities of Escherichia coli MRE600 ribosomes and fluorescently labeled E. coli mutant ribosomes in the PURExpress translation system and by determination of the 50% inhibitory concentrations (IC50) of three common macrolide antibiotics.
Funder
National Institutes of Health
Stanford University Center for Molecular Analysis and Design
Publisher
Cold Spring Harbor Laboratory
Cited by
20 articles.
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