posted on 2021-02-12, 19:04authored byLars K. Petersen, Allan B. Christensen, Jacob Andersen, Charlotta G. Folkesson, Ole Kristensen, Charlotte Andersen, Amaya Alzu, Frank A. Sløk, Peter Blakskjær, Daniel Madsen, Carlos Azevedo, Iolanda Micco, Nils J. V. Hansen
DNA-encoded small
molecule libraries (DELs) have facilitated the
discovery of novel modulators of many different therapeutic protein
targets. We report the first successful screening of a multimillion
membered DEL inside a living cell. We demonstrate a novel method using
oocytes from the South African clawed frog Xenopus laevis. The large size of the oocytes of 1 μL, or 100 000 times bigger
than a normal somatic cell, permits simple injection of DELs, thus
resolving the fundamental problem of delivering DELs across cell membranes
for in vivo screening. The target protein was expressed
in the oocytes fused to a prey protein, to allow specific DNA labeling
and hereby discriminate between DEL members binding to the target
protein and the endogenous cell proteins. The 194 million member DEL
was screened against three pharmaceutically relevant protein targets,
p38α, ACSS2, and DOCK5. For all three targets multiple chemical
clusters were identified. For p38α, validated hits with single
digit nanomolar potencies were obtained. This work demonstrates a
powerful new approach to DEL screening, which eliminates the need
for highly purified active target protein and which performs the screening
under physiological relevant conditions and thus is poised to increase
the DEL amenable target space and reduce the attrition rates.