D. Van Damme

The paper introduces PUP-IT, a pupylation-based proximity labelling method for detecting protein interactions in plants, and identifies BEN1 as a regulator of cellulose synthesis.

This study identifies TETRASPANIN1/TORNADO2 as a regulator of vascular proliferation and ground tissue patterning in Arabidopsis through transcriptomic analysis and mutant characterization.

The paper identifies SMB-controlled decompartmentalization events and ion fluxes in Arabidopsis root cap cells that execute programmed cell death.

This study shows that the nuclear matrix binding protein AHL22, along with FRS7 and FRS12, represses hypocotyl elongation in Arabidopsis by suppressing SAUR gene expression through chromatin attachment and histone deacetylation.

The paper investigates the role of TPLATE complex-dependent endocytosis in regulating CLAVATA1 signaling in Arabidopsis shoot apical meristem maintenance.

The paper introduces a phase separation-based method to visualize protein-protein interactions and kinase activities in plants using the SYMPL vector set.

The paper maps AP complex interactions in Arabidopsis, identifying P34 as a stability regulator of clathrin-mediated endocytosis and post-Golgi trafficking.

This study shows that a BR-binding-deficient BRI1 mutant is internalized similarly to wild-type BRI1, suggesting parallel endocytic routes and non-canonical functions.

This study shows that AtEH1 and AtEH2 subunits of the TPC complex drive biomolecular condensation to facilitate clathrin-mediated endocytosis in plants, with their disordered regions regulating condensate properties and endocytosis dynamics.

The paper identifies MYB12 as a repressor of TMO5/LHW-mediated transcription in Arabidopsis root meristems, revealing a negative feedback loop that regulates cell proliferation.

The paper characterizes the proteome of Arabidopsis clathrin-coated vesicles, identifying conserved and plant-specific components involved in clathrin-mediated trafficking.

The paper identifies the TPLATE complex as a mediator of membrane bending in plant clathrin-mediated endocytosis, which occurs independently of actin and against high turgor pressure.

The paper investigates how pharmacological and genetic manipulations of Ca2+ signaling affect auxin-regulated PIN trafficking, finding contrasting results between exogenous Ca2+ manipulations and genetic mutants.

The paper determines the structural architecture of the plant TSET complex and identifies key interactions essential for its assembly and function in endocytosis.

This study identifies distinct lipid and protein binding roles of EH domains in the TPLATE complex, revealing their functional contributions to plant clathrin-mediated endocytosis.

The paper establishes TurboID as the most effective PDL method in plant systems and demonstrates its utility in capturing protein interactomes and structural information.

The paper introduces a conditional in vivo PPI tool for plants, KSP, which allows visualization of protein-protein interactions and complex multi-protein interactions using rapamycin-dependent delocalization.

This study uses nanobody-dependent delocalization to reduce TPC function in Arabidopsis root cells, showing reduced endocytic flux without major growth effects.

The paper uses live cell imaging to show that the TPLATE complex is recruited to the plasma membrane as an octameric complex, not sequentially.

The paper identifies TPXL3 as the primary activator of α Aurora kinases in Arabidopsis, essential for embryogenesis, while TPX2 and TPXL2 have distinct roles.