Cell‐free bioluminescent screening of translation inhibitors

Abstract

The possibility of creating new screening methods with a cell‐free translation system has been demonstrated with a quantitative determination of diphtheria toxin and some antibiotics (puromycin, kanamycin and tetracycline) as examples. The approach proposed follows from the ability of various substances to inhibit protein synthesis. We used a wheat‐germ cell‐free translation system stabilized by freeze‐drying in the presence of trehalose with the mRNA of the Ca2+‐activated photoprotein obelin as a reporter template. This freeze‐dried cell‐free translation system allows prolonged storage of the detecting system before it is required, increases the reproducibility of the results and simplifies the application procedure. The obelin mRNA extends the sensitivity of the method owing to the high sensitivity of detection of the synthesized protein.