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Nature Communications|October 20, 2023
A conformation-locking inhibitor of SLC15A4 with TASL proteostatic anti-inflammatory activityAndras Boeszoermenyi, Léa Bernaleau, Xudong Chen, et al.Immunity|November 4, 2018
The T Cell Antigen Receptor α Transmembrane Domain Coordinates Triggering through Regulation of Bilayer Immersion and CD3 Subunit AssociationsKristine N Brazin, Robert J Mallis, Andras Boeszoermenyi, et al.Nature|March 11, 2020
An open-source drug discovery platform enables ultra-large virtual screensChristoph Gorgulla, Andras Boeszoermenyi, Zi-Fu Wang, et al.Cell Chemical Biology|July 29, 2023
Paralog-dependent isogenic cell assay cascade generates highly selective SLC16A3 inhibitorsVojtech Dvorak, Andrea Casiraghi, Claire Colas, et al.Biorxiv : the Preprint Server for Biology|April 1, 2024
"Multiplexed screen identifies a Pseudomonas aeruginosa -specific small molecule targeting the outer membrane protein OprH and its interaction with LPS"Bradley E Poulsen, Thulasi Warrier, Sulyman Barkho, et al.Cell Chemical Biology|December 28, 2024
Discovery of a Pseudomonas aeruginosa-specific small molecule targeting outer membrane protein OprH-LPS interaction by a multiplexed screenBradley E Poulsen, Thulasi Warrier, Sulyman Barkho, et al.Nature|February 18, 2016
Inhibiting fungal multidrug resistance by disrupting an activator-Mediator interactionJoy L Nishikawa, Andras Boeszoermenyi, Luis A Vale-Silva, et al.Nature Chemistry|May 5, 2025
Leveraging relaxation-optimized 1H-13CF correlations in 4-19F-phenylalanine as atomic beacons for probing structure and dynamics of large proteinsAndras Boeszoermenyi, Denitsa L Radeva, Sebastian Schindler, et al.Science (New York, N.Y.)|April 25, 2024
Large-scale chemoproteomics expedites ligand discovery and predicts ligand behavior in cellsFabian Offensperger, Gary Tin, Miquel Duran-Frigola, et al.Pageof 3