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. Author manuscript; available in PMC: 2015 Mar 30.
Published in final edited form as: J Biomol Screen. 2014 Aug 27;20(1):122–130. doi: 10.1177/1087057114548832

Figure 1.

Figure 1

T. brucei MetRS catalyzed reaction. The primary screen assay focuses on the luminescence signal generated from the luciferase catalyzed reaction using residual ATP. The orthogonal counterscreen focuses on the fluorescence polarization signal generated from the displacement of a labeled AMP molecule from a selective antibody when AMP is generated from the T. brucei MetRS catalyzed reaction.