Design of Signal Windows in High Throughput Screening Assays for Drug Discovery

Author:

Sittampalam G. Sitta1,Iversen Philip W.2,Boadt Joyce A.1,Kahl Steven D.1,Bright Stuart1,Zock Joseph M.3,Janzen William P.4,Lister Mark D.4

Affiliation:

1. Technology Core Research Division, Lilly Research Laboratories, Eli Lilly & Company, Indianapolis, IN 46285

2. Statistical & Mathematical Sciences, Lilly Research Laboratories, Eli Lilly & Company, Indianapolis, IN 46285

3. Natural Products Research, Lilly Research Laboratories, Eli Lilly & Company, Indianapolis, IN 46285

4. Sphinx Pharmaceuticals Corporation, A Division of Eli Lilly & Company, 4615 University Drive, Durham, NC 27707

Abstract

High Throughput Screening (HTS) assays are used to rapidly identify promising drug candidates or leads from hundreds of thousands of compounds. Hence, it is important that the assay should be designed to discriminate responses from the active and inactive compounds and the background noise. We introduce the idea of a signal window which provides a degree of separation between signals. This allows one to correctly identify new molecular entities with desired level of activity (called "hits") in the presence of variability. The statistical criteria for setting and calculating signal windows are presented along with illustrative examples. Results show that the ideal signal window should be 2 standard deviations (SD) of the largest signal in screening assays, although a 1 SD window size is the minimum acceptable limit. When signal windows are set below 2 SD, the probability of missing "hits" increases significantly.

Publisher

Elsevier BV

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