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Promega webinar: NanoBRET: A Quantitative Technique to Measure Kinase Target Engagement in Live Cells

Although a number of extracellular techniques exist to quantitatively measure kinase-ligand binding or inhibition, until now there was no means by which to quantitate target occupancy or drug affinity in live cells. In this webinar we report the use of an energy transfer technique (NanoBRET) in the first quantitative approach to profiling kinase occupancy of a test compound inside live cells.

Intracellular target selectivity is a key aspect of pharmacological mechanism. Although a number of acellular techniques have been developed to quantitatively measure kinase binding or enzymatic inhibition, currently no biophysical approaches exist that offer quantitative analysis of target occupancy or drug affinity in live cells. Here we report the application of an energy transfer technique (NanoBRET) that enables the first quantitative approach to broadly profile kinase occupancy under thermodynamic equilibrium with the test compound inside live cells. This approach enabled a mechanistic interrogation of the potency offsets observed between cellular and acellular analysis of kinase engagement, and uncovered improved intracellular selectivity profiles for certain clinically-relevant multi-kinase inhibitors. The energy transfer technique can also be performed in real time, enabling assessments of compound residence time. Applications of NanoBRET for the measurements of target engagement and residence time for ATP-competitive and non-competitive inhibitors will be presented.

Speaker Bio:

Matthew Robers is a Senior Research Scientist and Group Leader at Promega Corporation.  Matthew has authored over 25 peer-reviewed publications and published patents on the application of novel assay chemistries to measure intracellular protein dynamics. Matthew's team currently focuses on the development of new technologies to assess target engagement, and has developed a biophysical technique for quantifying compound affinity and residence time at selected targets within intact cells.

View webinar recording here
23 January 2018

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