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Ben Lehner

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Open access Sep 2026

Multimodal allostery in a single-domain protein

Allosteric communication between distant sites in proteins is central to biological regulation and underlies the efficacy of many drugs. Allostery allows proteins to function as molecular switches, with their activities controlled by ligand binding, covalent modifications, and mutations outside their active sites. Allo...

Yu-Jing Ma, Qi-Le Jin, Ben Lehner et al. · 0 citations
Open access Aug 2026

Proteome-wide identification of the druggable CRBN interactome.

This pipeline identified 6 known and 43 novel CRBN-pomalidomide binders, including orthogonally validated hits that provide privileged starting points for MGD development, and expects this binding-focused workflow to be applicable to other MGD-E3 ligase systems, potentially extending the scope of this emerging drug cla...

Pius Galli, Shuhao Xiao, Y. Meng et al. · 1 citation
Open access Aug 2026

Conservation and divergence in the allosteric architectures of five human protein kinases

The activity and abundance of >160,000 variants are quantify the activity and abundance of >160,000 variants to construct complete maps of the energetic and allosteric architectures of five human kinase domains: SRC, FGR, JNK2/MAPK9, ZAK/MAP3K20, and TSSK2.

Carla Folgado, Antoni Beltran, Ben Lehner · 0 citations
Open access Jul 2026

The genetic architecture of human programmed stop codon readthrough

This study provides comprehensive quantitative maps of the sequence determinants of human programmed readthrough and suggests that three examples of programmed readthrough are located on distinct local fitness peaks, each defined by different upstream and downstream architectures built around a shared CUAG core motif.

Ignasi Toledano, Fran Supek, Ben Lehner · 0 citations

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