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Unité du Prof. Barth

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From Sequence to Dynamics to Function: Computational Design of Allostery and Ligand Selectivity in G-Protein Coupled Receptors

Computational rewiring of allosteric pathways reprograms GPCR selective responses to ligands

Computationally designed GPCR quaternary structures bias signaling pathway activation

Reprogramming G Protein-Coupled Receptor Structure, Function And Signaling By Computational Design

Computational design of highly signaling active membrane receptors through de novo solvent-mediated allosteric networks

Computationally designed GPCR quaternary structures bias signaling pathway activation

Enhancing the Signaling of GPCRs via Orthosteric Ions

Functional de novo Protein Design for Targeted Vaccines and Synthetic Biology Applications

Computational design of G Protein-Coupled Receptor allosteric signal transductions

Cytosolic delivery and characterization of monobodies interfering with SH2 domain-phosphotyrosine interactions

Computationally designed GPCR quaternary structures bias signaling pathway activation

From Sequence to Dynamics to Function: Computational Design of Allostery and Ligand Selectivity in G-Protein Coupled Receptors

Functional de novo Protein Design for Targeted Vaccines and Synthetic Biology Applications

Computational design of G Protein-Coupled Receptor allosteric signal transductions

Enhancing the Signaling of GPCRs via Orthosteric Ions

Computational design of highly signaling active membrane receptors through de novo solvent-mediated allosteric networks

Computationally designed GPCR quaternary structures bias signaling pathway activation

Cytosolic delivery and characterization of monobodies interfering with SH2 domain-phosphotyrosine interactions

Computational rewiring of allosteric pathways reprograms GPCR selective responses to ligands

Reprogramming G Protein-Coupled Receptor Structure, Function And Signaling By Computational Design