bioRxiv Science⌕ Search

Biology subjects

Kramer, T. W.

Publications and source records attributed to Kramer, T. W..

2 recordsLinked to original sources

Development of NanoBRET cellular target engagement assays in primary neurons for activating mutants of p21-activated kinase 1

The p21-activated kinases (PAKs) are a group of serine-threonine kinases central to multiple signaling pathways that govern cell survival and proliferation. Aberrant activity of PAK1, the most well characterized member of the PAK family, drives progression of several malignancies and brain disorders, including Alzheimers disease and neurodevelopmental disorders. Despite growing interest in PAK1 as a drug target for these diseases, there is no assay to evaluate the intracellular target engagement of PAK1 inhibitors. To address this need, we developed first-in-class NanoBRET assays for wild-type PAK1 and a neurodevelopmental disorder-causing gain-of-function PAK1 mutant. Furthermore, we executed our novel PAK1 NanoBRET assay to evaluate target engagement of PAK1 inhibitors in primary hippocampal neurons. To the best of our knowledge, this is the first demonstration of a NanoBRET cellular target engagement assay in primary neurons, thereby increasing the relevance of our work by confirming PAK1 inhibitor binding to the aberrant form of the protein in primary neurons.

pharmacology and toxicology↗

Development of a chemical probe to enable characterization of the casein kinase 1γ subfamily

The casein kinase 1{gamma} (CK1{gamma}) subfamily, while severely understudied, is implicated in diverse disease-relevant pathways, including WNT signaling and human cytomegalovirus (HCMV) replication. While genetic tools exist to study CK1{gamma}, the selective inhibition of CK1{gamma} through pharmacological means remains underexplored. Chemical probes, or potent and selective inhibitors, remain one of the most powerful pharmacological tools for uncovering protein biology. Herein, we developed several novel assays for assessing target engagement with the CK1{gamma} subfamily in cells. Enabled by these assays, we conducted a comprehensive structure-activity relationship (SAR) campaign to develop the first chemical probe, SGC-CK1{gamma}-1, for the CK1{gamma} subfamily. SGC-CK1{gamma}-1, which was developed alongside a structurally related negative control compound, potently and selectively inhibited the CK1{gamma} kinases in living cells, plus inhibited both WNT signaling and human cytomegalovirus replication.

pharmacology and toxicology↗